| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs3693074 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Ppp1r13b | Mm_Celera | 12:111844508 | GAAAGAATTATGAAC[C/T]TCCTGATTAAGCAAT | 21981 |
| rs4137171 | snp | A/T | 0.484429 | 0.0868505 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111844291 | TTACAGGCATGTGCC[A/T]CCATACCTGGCAGTA | 21981 |
| rs6333099 | snp | C/T | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111853032 | TTCCTAATTTCCCTA[C/T]ACCCCAAATCCACTG | 21981 |
| rs13464475 | snp | C/T | | | synonymous-codon | Ppp1r13b | GRCm38.p3 | 12:111833131 | TCCTCCAGCAGCATC[C/T]GCGGTGGGTATCCTT | 21981 |
| rs13474523 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Ppp1r13b, Zfyve21 | Mm_Celera | 12:111828675 | GATTGTTTTTCAGCC[A/G]GGCCACTGGAACTGT | 21981 |
| rs13481654 | snp | C/T | 0.499541 | 0.0151446 | synonymous-codon | Ppp1r13b | GRCm38.p3 | 12:111835205 | AGAGCTTGTTGATCC[C/T]GGGCCCAAGGGCCCA | 21981 |
| rs29123704 | snp | C/T | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111841708 | CTAGCCTTGGCTACA[C/T]GCACACTAAGTTCAG | 21981 |
| rs29124235 | snp | C/T | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111841930 | CTACAGAGAGAGTTC[C/T]AGGACAGCCAGGGAA | 21981 |
| rs29127356 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ppp1r13b | Mm_Celera | 12:111891026 | GGAACGAGTCAGGCA[C/T]GGGAGATTCACCCCA | 21981 |
| rs29127790 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | Mm_Celera | 12:111907347 | TAAAGGAAAAGGCAA[A/G]GAAGGTGGCAACCCC | 21981 |
| rs29128185 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111869309 | GCTCAGTTGGAAGAA[C/T]GTTTGCCTAGCTTGT | 21981 |
| rs29128369 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Ppp1r13b | Mm_Celera | 12:111869687 | CAGAGTCTAGCTGAA[A/G]CTCCTGACCTGCTCT | 21981 |
| rs29129988 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111856640 | GTTGTAGGCTTGTAT[G/T]GTAGTAGAGATGGAA | 21981 |
| rs29132901 | snp | A/T | 0.484429 | 0.0868505 | intron-variant | Ppp1r13b | Mm_Celera | 12:111860366 | AGAAGAAACCATCCT[A/T]AACTGGAGAGTGAAA | 21981 |
| rs29133282 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111875241 | GCATGTGAACACACA[C/G]ACACATGAACATACA | 21981 |
| rs29137564 | snp | A/G | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111882939 | AAGATGTGAGCTATT[A/G]TTTTTAAATGTTTCT | 21981 |
| rs29137597 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111862811 | GCAAAGCAAGGCCAC[A/G]TGAAACTTGCTTTGA | 21981 |
| rs29137870 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | Mm_Celera | 12:111860648 | TGTATTGCTTTCCTG[C/T]CTTCTGGAGGAAAGA | 21981 |
| rs29138507 | snp | A/T | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111900619 | TTCTTATAACAAAAA[A/T]CTCCTTCTCCCTTCA | 21981 |
| rs29140202 | snp | A/T | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111882503 | CGAGGTTGAGGCTAG[A/T]CTGGGCTACACAGCT | 21981 |
| rs29141516 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | Mm_Celera | 12:111874782 | ACACAGTAGAACTCT[C/T]GTCTCAACATCAAAA | 21981 |
| rs29142131 | snp | A/T | 0.5 | 0 | intron-variant | Ppp1r13b | Mm_Celera | 12:111898691 | TCAGGGGTGGTGGCG[A/T]GCATTTACCTCTAAG | 21981 |
| rs29142452 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ppp1r13b | Mm_Celera | 12:111842010 | AGGGTTATAGAATAA[C/T]AGGGTCAGCAAGGAA | 21981 |
| rs29142919 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111869912 | CACAAGTTTAATCTC[A/G]TTGTTACTACTCTTA | 21981 |
| rs29143230 | snp | C/T | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111857052 | TCCATGGGCCCTGCT[C/T]ATGCACATGGTGTAC | 21981 |
| rs29143778 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ppp1r13b | Mm_Celera | 12:111896779 | GCTCCATCACCTCCA[C/T]CCTTCCAGAGCTCTC | 21981 |
| rs29144077 | snp | A/G | 0.429688 | 0.173817 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Ppp1r13b, Zfyve21 | GRCm38.p3 | 12:111828364 | GTATATAAAGTGTAT[A/G]ATTAAAACTTATTTT | 21981 |
| rs29144924 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111884521 | GCAAGGGTATAGACC[C/T]GATCTGCACCTTGGG | 21981 |
| rs29148349 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111906475 | TCAACATGGAGCCAG[C/T]AAGAAAAGGGAAGAA | 21981 |
| rs29149019 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111845527 | TTTAAATTGTGAAAC[A/G]TTTTGTAAAGAACAG | 21981 |
| rs29149779 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ppp1r13b | Mm_Celera | 12:111844003 | CCAGGCTTTGACAGC[C/T]GTGCTGTGACTCCTC | 21981 |
| rs29150529 | snp | A/C | 0.5 | 0 | intron-variant | Ppp1r13b | Mm_Celera | 12:111854881 | ACACACACAAACACA[A/C]ACACACACACAGACA | 21981 |
| rs29150916 | snp | A/G | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111905944 | CTTTGGATACATGGT[A/G]TAAGATATTATGAAG | 21981 |
| rs29152901 | snp | A/T | 0.5 | 0 | intron-variant | Ppp1r13b | Mm_Celera | 12:111900411 | AACGTTATCTTTAAT[A/T]TAGCAAATAAAGGAT | 21981 |
| rs29153647 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Ppp1r13b | Mm_Celera | 12:111851251 | TTTATACATTTTTTT[C/T]CTGTATGGATAGTTC | 21981 |
| rs29154057 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111905772 | TTTACTTTTATAGTA[C/T]CTAAGGTATTTTATA | 21981 |
| rs29154556 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111883031 | AGGGAAATACCCGAG[C/T]AGATGACCTGGAGGT | 21981 |
| rs29154636 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111845543 | TTTTGTAAAGAACAG[A/G]ACAATCCTACAGGAA | 21981 |
| rs29156449 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111860819 | AACAGTGATCTTGCC[C/T]TTGAGAATGTCCATG | 21981 |
| rs29157453 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111899473 | GAGTGTCACCTTGTC[A/G]TACTCTAAAGTCATG | 21981 |
| rs29158728 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Ppp1r13b | Mm_Celera | 12:111854945 | TTCTTACTGTGATGT[A/G]TGCCCTGTGTCCTGG | 21981 |
| rs29158860 | snp | C/T | 0.5 | 0 | intron-variant | Ppp1r13b | Mm_Celera | 12:111884801 | CTGTATCATGAATGG[C/T]TAGCTGCTGGGTGTT | 21981 |
| rs29158919 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111907310 | GAATTCAGCATCCAC[C/T]GCTGCTTGTACCGCA | 21981 |
| rs29160349 | snp | A/T | 0.487535 | 0.077957 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111882324 | TTTTAAAAGCCCAGA[A/T]CTATGTGATTATGTA | 21981 |
| rs29160589 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111906683 | GTCAAGGACACAATA[C/T]GAAGAGGTACCAGAA | 21981 |
| rs29162150 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111875211 | CACAAACATATTTGA[C/T]ATACACATGCATAGG | 21981 |
| rs29162772 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111861976 | GGTGCACAGATGTGG[A/G]TGCAGGCAAAATATC | 21981 |
| rs29165521 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111835402 | TACAATTTGTAAGCC[A/G]TTAAAGGACATAGGA | 21981 |
| rs29165834 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Ppp1r13b | Mm_Celera | 12:111866267 | ACAAGCCCTCGCTTG[C/T]TGAGGCAGGTAGTCC | 21981 |
| rs29166160 | snp | C/T | 0.5 | 0 | intron-variant | Ppp1r13b | Mm_Celera | 12:111900269 | ACACACACACACACA[C/T]ACACACACACAGTTT | 21981 |
| rs29166426 | snp | A/T | 0.5 | 0 | intron-variant | Ppp1r13b | Mm_Celera | 12:111880511 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 21981 |
| rs29166860 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | Mm_Celera | 12:111841455 | TACTGTCTCCCAATT[A/T]AAAAAAATTAATAAA | 21981 |
| rs29167172 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111865255 | ATATATCCACCCATA[C/T]TGTCAGGATGCTTAC | 21981 |
| rs29167336 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ppp1r13b | Mm_Celera | 12:111891097 | ACTAGCCATGTGGAA[A/G]ACATAAAATAGAATA | 21981 |
| rs29169646 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111905836 | AGTCCTACTGCTTTG[A/T]ACAACCACAGCATAA | 21981 |
| rs29170333 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111861346 | GAATTCAGGTCCTCT[A/G]GAAGAGGAGCTGTTG | 21981 |
| rs29170434 | snp | A/T | 0.487535 | 0.077957 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111881101 | CAATTAGCCAGGTTA[A/T]ACCTAATGCTTTTAT | 21981 |
| rs29170990 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Ppp1r13b | Mm_Celera | 12:111870436 | ATCCATGGTAGGCAA[A/G]CCCTGCCTTACCTGC | 21981 |
| rs29172086 | snp | A/C | 0.5 | 0 | intron-variant | Ppp1r13b | Mm_Celera | 12:111869680 | CCCAGCCCAGAGTCT[A/C]GCTGAAGCTCCTGAC | 21981 |
| rs29172185 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111841563 | ACGTGATAAAATGGC[C/T]GATGCTGAAGAGTCT | 21981 |
| rs29172324 | snp | A/G | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111829898 | CTACCAAAGCACTAC[A/G]AGAACAGCAACAACA | 21981 |
| rs29172533 | snp | A/C/G | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111854875 | ACACACACACACACA[A/C/G]ACACACACACACACA | 21981 |
| rs29173434 | snp | G/T | 0.5 | 0 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Ppp1r13b, Zfyve21 | GRCm38.p3 | 12:111828081 | AGAAGCTGCACTACA[G/T]TACTGCTAAACCAGG | 21981 |
| rs29173687 | snp | C/G | 0.475309 | 0.108333 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111843988 | GGCTGCAAAACACCA[C/G]CAGGCTTTGACAGCT | 21981 |
| rs29174720 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111862685 | TAGGATAGTAAGTAA[C/T]GGCTGCATAATAAAG | 21981 |
| rs29175283 | snp | A/G | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111905736 | CTAACAAAAAGGTAT[A/G]TAGAGAACTACTTGG | 21981 |
| rs29176000 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111882979 | AAACTCAGCAAGAGT[A/G]TAGTATAGAGCACAC | 21981 |
| rs29176042 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | Mm_Celera | 12:111899294 | AATCTTGTGCTTAAA[C/T]ATGAGCTCAAGTTCC | 21981 |
| rs29177083 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111880797 | TTCTCACACCCTTAA[C/T]TTCTGTCTTTACTCT | 21981 |
| rs29179311 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111865587 | GGGGTTACAGGTGTG[C/T]ACCACCATGGACGGC | 21981 |
| rs29182615 | snp | A/C | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111858866 | CCATCACATGCGACT[A/C]TTTCTAGCTGTACGT | 21981 |
| rs29183147 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111829581 | TAGCACCCATGCTTG[C/G]CTCATACTTTGCCAG | 21981 |
| rs29183435 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111860542 | TTGTATAATTTAATA[C/T]ACAAAAACCAAGGGC | 21981 |
| rs29185392 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Ppp1r13b | GRCm38.p3 | 12:111909655 | AGCTCTGCTTCATTT[C/T]CTGCGAGGTCTCAGG | 21981 |
| rs29186302 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111850951 | CAAAGCTAAAACAAA[C/T]AACATAGGATTGGTT | 21981 |
| rs29186910 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | Mm_Celera | 12:111881302 | ATCCCAGCACTTGGG[A/T]GTCAGAGGCAGGCAG | 21981 |
| rs29187228 | snp | A/C | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111870029 | ATCCCCTGCTTCAGC[A/C]TTCTCATGCTGGGAT | 21981 |
| rs29187616 | snp | C/T | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111884735 | AATTAATAAAACACA[C/T]AGCTAATGTGAGTTT | 21981 |
| rs29187679 | snp | G/T | 0.611111 | 0.124226 | intron-variant | Ppp1r13b | Mm_Celera | 12:111887648 | ATATAAAAATAAAAA[G/T]ACCTAACTGTCTTAG | 21981 |
| rs29188040 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111899274 | ATGATGCATGGGAAA[A/C]AACAAATCTTGTGCT | 21981 |
| rs29193400 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111829750 | CAATCAGGTCTCTAA[C/G]CACGGCTGCGTTAAC | 21981 |
| rs29194769 | snp | A/G | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111864376 | GGCAGCACTAAGACT[A/G]CATGCACACTGCCTG | 21981 |
| rs29194824 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111862699 | ATGGCTGCATAATAA[A/G]GAATACAATGAACTT | 21981 |
| rs29195567 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111838412 | ATGATCCAACCCAAG[C/T]TTGTGGATTTCTGAC | 21981 |
| rs29195735 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | Mm_Celera | 12:111859717 | GTCCTGGAATTTATA[A/T]AAGGCAGGTATATTT | 21981 |
| rs29195802 | snp | A/T | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111885808 | ATCCCCAGGGCCCAG[A/T]CAGCGGGCTAGAACT | 21981 |
| rs29198561 | snp | A/G | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111859025 | CAGTGTGAGCTCTGA[A/G]CCACTGAGATGACTC | 21981 |
| rs29198817 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111856369 | CAGGTTCTATGGTAG[C/T]TATCTATAAAACTTA | 21981 |
| rs29199310 | snp | C/T | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111858741 | TGTTTTTTGAGAAGA[C/T]GAGGTCTTGCTATAT | 21981 |
| rs29200031 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111899355 | TCCAGGGGAATAAGA[A/C/G]TTAAATCAGAGACTC | 21981 |
| rs29200839 | snp | C/T | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111858766 | CTATATTATACAGCC[C/T]TGGCTGGCTGGAACT | 21981 |
| rs29203779 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111835559 | AGCTGAAGATCAGAA[C/T]ATAAGGGAAACTCCC | 21981 |
| rs29205654 | snp | A/G | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111870129 | TGCTTTTATTTATTT[A/G]TTAAATATTCAATTT | 21981 |
| rs29205689 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111838396 | GCTTCGCAGCCACCC[C/T]ATGATCCAACCCAAG | 21981 |
| rs29206851 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ppp1r13b | Mm_Celera | 12:111869748 | CCGACACAGGGATGT[C/T]TTATATACTTCATGT | 21981 |
| rs29206907 | snp | C/T | 0.456747 | 0.140554 | utr-variant-3-prime, downstream-variant-500B | Ppp1r13b, Zfyve21 | GRCm38.p3 | 12:111828519 | GCACTGGGATGGCAG[C/T]GGCTGCTCACGGGTG | 21981 |
| rs29207829 | snp | G/T | 0.456747 | 0.140554 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111860934 | GGCTCCGAATCTTTC[G/T]AATGGACATATACAT | 21981 |
| rs29209859 | snp | A/G | 0.5 | 0 | intron-variant | Ppp1r13b | GRCm38.p3 | 12:111841395 | CTGGAAGCAGAGGCA[A/G]GTGGCTATCTGTGAG | 21981 |
| rs29210264 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Ppp1r13b | Mm_Celera | 12:111859443 | CCACATCCTTTCCAG[A/G]GGAATCTCGAGGCAG | 21981 |
| rs29212719 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ppp1r13b | Mm_Celera | 12:111851048 | TTTTTTTAAAGATTT[A/C]TTATTATATGTAAGT | 21981 |