| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs3139037 | snp | A/T | | | intron-variant | ? | WS195 | I:12738895 | ATCAACTAGTCTTTT[A/T]CTATAAAAACATGGT | 173144 |
| rs193577862 | snp | C/T | | | intron-variant, synonymous-codon | ? | WS195 | I:12738112 | CTCCGCACCGCTTCT[C/T]GTCGACCCGAGCACA | 173144 |
| rs193577864 | snp | C/T | | | missense, intron-variant | ? | WS195 | I:12738960 | AATTTCAGGAACTGC[C/T]CGACCAATCATCACT | 173144 |
| rs193577865 | snp | A/C | | | intron-variant | ? | WS195 | I:12740382 | TTGAAAATTGCTGTT[A/C]TCACTGAAAAATGCG | 173144 |
| rs353120836 | snp | G/T | | | intron-variant | ? | WS195 | I:12739875 | CTGGAGCAGTTTCAC[G/T]TGGTGGTGAAGTGTC | 173144 |
| rs353129209 | snp | A/T | | | utr-variant-3-prime, intron-variant | ? | WS195 | I:12741130 | AGTCAATAAAAATTT[A/T]ATTTTTTTAAAGATT | 173144 |
| rs353132490 | snp | C/T | | | intron-variant | ? | WS195 | I:12739854 | ATTTTGAGAATTTTA[C/T]TGGTTCTGGAGCAGT | 173144 |
| rs353152020 | snp | A/G | | | intron-variant | ? | WS195 | I:12740098 | AAAATTGAGCACTTT[A/G]AAGCTCCGAAAGTAT | 173144 |
| rs353160239 | snp | C/T | | | intron-variant | ? | WS195 | I:12738273 | CGCCGAGGGTGAGTA[C/T]CATTTTGGTCATTTC | 173144 |
| rs353169533 | in-del | -/T | | | intron-variant | ? | WS195 | I:12739664 | GTGAGTTCTTTTTTC[-/T]TTTTTTGAGCTATTT | 173144 |