| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193345384 | snp | A/T | 0.148556 | 0.228493 | missense | ? | WS195 | V:5045535 | CTTACCCTGGACTAT[A/T]ATGTTTCCTGCTCGA | 178892 |
| rs193345385 | snp | C/T | 0.01005 | 0.0701712 | intron-variant | ? | WS195 | V:5045716 | CTTTATTTGATCCTA[C/T]ACGAAATTAAACATT | 178892 |
| rs193619769 | snp | A/T | | | intron-variant | ? | WS195 | V:5044580 | GGTCAGGAACATTTA[A/T]TGTGTTAGTTTTACT | 178892 |
| rs193619770 | snp | A/G | | | intron-variant | ? | WS195 | V:5044718 | AATGTCAACTAAAGT[A/G]CACACTTACATTCAG | 178892 |
| rs193619771 | snp | C/T | | | intron-variant | ? | WS195 | V:5044825 | TTTCGTACAAAAATA[C/T]GGTACCCGGTCTCGG | 178892 |
| rs193619772 | snp | C/T | | | intron-variant | ? | WS195 | V:5044878 | TCAGAAAGTGCGCTC[C/T]TTTAAAGATTACTGT | 178892 |
| rs193619773 | snp | A/C | | | intron-variant | ? | WS195 | V:5046111 | GACTCGAAAATCCAA[A/C]TGAAAAAAGCGCCAA | 178892 |