Gm16381
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs45828026snpA/C0.320.24upstream-variant-2KBGm16381GRCm38.p312:87650499CAACTCATGTAAGAA[A/C]AAAAGATGGATGTAA100042786
rs47496654snpA/Tintron-variantGm16381GRCm38.p312:87644762AAAGCACTCGAACAC[A/T]GAAAGATGAAGATGA100042786
rs48179851snpA/G0.4977780.0332592upstream-variant-2KBGm16381GRCm38.p312:87650732TCTGCCTGCCAAGAA[A/G]CATCCAACAACAACT100042786
rs48963239snpA/C/G/Tupstream-variant-2KBGm16381GRCm38.p312:87650181TAATCCGAGGACTCT[A/C/G/T]AGTTCAATGTCAGCC100042786
rs49127080snpC/Tupstream-variant-2KBGm16381GRCm38.p312:87650130GTCTATATATAGTGG[C/T]ACACACCTTTAATCT100042786
rs49465730snpA/Gupstream-variant-2KBGm16381GRCm38.p312:87650230AGGTAATGGCCATGA[A/G]AAACTTAGGCCCAGG100042786
rs49517315snpG/Tupstream-variant-2KBGm16381GRCm38.p312:87650617TGTGGCGTTTGTTGT[G/T]CTGGGTGCCCTCTGT100042786
rs50123772snpC/Tupstream-variant-2KBGm16381GRCm38.p312:87650696CAGGCTTTACCTGCC[C/T]GTGGATCTTTGAGAG100042786
rs50820055snpA/Gupstream-variant-2KBGm16381GRCm38.p312:87650112ACACCTTTAATCTAG[A/G]CCACACCTTCTGCTA100042786
rs51330052snpA/Gupstream-variant-2KBGm16381GRCm38.p312:87650153GCCTGGGACAAAGCA[A/G]GTCCCAGGTCTATAT100042786
rs51492811snpA/C/G/Tupstream-variant-2KBGm16381GRCm38.p312:87650393TCACTGCAACTTCCT[A/C/G/T]ACAACTTTGAGTTTC100042786
rs51949822snpG/Tintron-variantGm16381GRCm38.p312:87644761AAGCACTCGAACACT[G/T]AAAGATGAAGATGAA100042786
rs107918007snpC/Tupstream-variant-2KBGm16381GRCm38.p312:87650892TTTTGGTTTTTTTTT[C/T]TTTCTTTCTTTCTTT100042786
rs108073605snpG/Tupstream-variant-2KBGm16381GRCm38.p312:87650880TGGTTTTTGTTTTTT[G/T]GGTTTTTTTTTTTTT100042786
rs108261610snpC/Tupstream-variant-2KBGm16381GRCm38.p312:87650964CTGTCCTGGAACTCA[C/T]TTTGTAGACCAGGCT100042786
rs108390908snpA/Tupstream-variant-2KBGm16381GRCm38.p312:87650766AAGGTCTGAATATGG[A/T]TAGCCTAGGGAGTGG100042786
rs108761184snpA/Gupstream-variant-2KBGm16381GRCm38.p312:87650742AAGAAGCATCCAACA[A/G]CAACTGTCAAGGTCT100042786
rs108889507snpG/Tupstream-variant-2KBGm16381GRCm38.p312:87650707CCACAGGCAGGTAAA[G/T]CCTGAATTGTCTGCC100042786
rs219568881snpA/Cupstream-variant-2KBGm16381GRCm38.p312:87650292CAATTTACAAAAAAA[A/C]CCAAAACCAAAAAAA100042786
rs220422926snpA/Gintron-variantGm16381GRCm38.p312:87645550TAGATAGGTAGATAG[A/G]TAGATAGATAGATAG100042786
rs223944445snpA/Cintron-variantGm16381GRCm38.p312:87645306TTAAAATACTCAAAC[A/C]AAAAAAAAAAAAAAG100042786
rs242370284snpC/Tintron-variantGm16381GRCm38.p312:87645417CCACAAGTAAAGGAA[C/T]CTAATTTCTTTCCTA100042786
rs246051305snpA/Gupstream-variant-2KBGm16381GRCm38.p312:87650142TGTACCACTATATAT[A/G]GACCTGGGACCTGCT100042786
rs250677119snpC/Tintron-variantGm16381GRCm38.p312:87645439TCTTTCCTACTTGTC[C/T]ATCTTTAAAATAACA100042786
rs387173856in-del-/Gupstream-variant-2KBGm16381GRCm38.p312:87650340CCTTAAAAAAAGCCA[-/G]AAGACCTAACTTCTC100042786
rs579194454snpA/Cupstream-variant-2KBGm16381GRCm38.p312:87650273TGTCAGCCCTGGTCC[A/C]CAGCAATTTACAAAA100042786
rs579647999snpA/Tupstream-variant-2KBGm16381GRCm38.p312:87650420GTGAGCTGACAGGGC[A/T]GAGGAGGAGGTTGCT100042786
rs580172822snpC/Gupstream-variant-2KBGm16381GRCm38.p312:87650438GGAGGAGGTTGCTCA[C/G]TCAGTGCAGTACTCA100042786
rs580868317snpA/C/Tupstream-variant-2KBGm16381GRCm38.p312:87650938GACAGGGTTTCCCTA[A/C/T]ATAGCCCTGGCTGTC100042786
rs581481167snpA/Tupstream-variant-2KBGm16381GRCm38.p312:87650601CAAGCAAACTTGCCC[A/T]ACAGAGGGCACCCAG100042786
rs582642694snpC/Tintron-variantGm16381GRCm38.p312:87645280TTCTAGTTACACTTC[C/T]ATTGCTGCTGTTAAA100042786
rs582650183snpA/Gupstream-variant-2KBGm16381GRCm38.p312:87650344TAAAAAAAGCCAAAG[A/G]CCTAACTTCTCTCTG100042786
rs583417654snpA/Gupstream-variant-2KBGm16381GRCm38.p312:87650424GCTGACAGGGCTGAG[A/G]AGGAGGTTGCTCACT100042786
rs583660639snpC/Tupstream-variant-2KBGm16381GRCm38.p312:87650487TTGAGTTCAATGCAA[C/T]TCATGTAAGAAAAAA100042786
rs585896265snpG/Tupstream-variant-2KBGm16381GRCm38.p312:87650433GCTGAGGAGGAGGTT[G/T]CTCACTCAGTGCAGT100042786
rs586631204snpC/Tupstream-variant-2KBGm16381GRCm38.p312:87650636ACAAACGCCACATGC[C/T]CAGTGTGTCTGTGCT100042786
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