| SNP - dbSNP | | dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs3139659 | snp | A/T | | | intron-variant | H24G06.1, ? | WS195 | V:9455005 | AATCCCTAGTTTACA[A/T]CATTGATTTTTCAGA | 179326 | | rs193346861 | snp | G/T | 0.0584834 | 0.16069 | missense | H24G06.1, ? | WS195 | V:9447130 | TATCAATTCAAAAAT[G/T]TTTTTGTTCAGTATG | 179326 | | rs193346862 | snp | A/G | 0.0198985 | 0.097741 | missense | H24G06.1, ? | WS195 | V:9448260 | ACATCAGTCTGCCAT[A/G]AAGTCAATCAAATTT | 179326 | | rs193346863 | snp | C/T | 0.0198985 | 0.097741 | intron-variant | H24G06.1, ? | WS195 | V:9448290 | TGCTTCGGTAAGATT[C/T]ATTTTTATTTAAATA | 179326 | | rs193346864 | snp | A/T | 0.0399833 | 0.135621 | intron-variant | H24G06.1, ? | WS195 | V:9449563 | AAATAACATTTTTTT[A/T]ATTCTATTTTTTTCA | 179326 | | rs193346865 | snp | A/G | 0.019998 | 0.0979748 | intron-variant | ?, H24G06.1 | WS195 | V:9450388 | TATGAAACATGGCCA[A/G]ATTTGAATTCATAAC | 179326 | | rs193346866 | snp | C/T | 0.0489887 | 0.148642 | intron-variant | H24G06.1, ? | WS195 | V:9450448 | CGCCAAGTATTTACA[C/T]TGTCAAGAAATTTTT | 179326 | | rs193346867 | snp | A/G | 0.0198 | 0.0975088 | intron-variant | ?, H24G06.1 | WS195 | V:9456188 | GTTTCTATGAATTCT[A/G]AATGAATTGGTATTT | 179326 | | rs193346868 | snp | C/T | 0.13875 | 0.223883 | intron-variant | H24G06.1, ? | WS195 | V:9459492 | AAAGTTTGAGTTTCA[C/T]CAAATTATCTGCATT | 179326 | | rs193622870 | snp | A/C | | | missense | H24G06.1, ? | WS195 | V:9446622 | GGCAACTTCGTGATG[A/C]ACAAGGCAATTTTGT | 179326 | | rs193622871 | snp | C/G | | | intron-variant | H24G06.1, ? | WS195 | V:9452208 | TTTTGTTCTTTTAAA[C/G]ATGTTTCTAATAAAG | 179326 | | rs193622872 | snp | C/T | | | intron-variant | ?, H24G06.1 | WS195 | V:9452306 | AGTTCGTAGAATTTT[C/T]AGGTTTGAGATTATT | 179326 | | rs193622873 | snp | G/T | | | intron-variant | H24G06.1, ? | WS195 | V:9452541 | CACAAACCTAATCAC[G/T]TTGCGGAAACGCTCA | 179326 | | rs193622874 | snp | C/G | | | utr-variant-5-prime, missense | ?, H24G06.1 | WS195 | V:9454806 | CAAACCTCGGAAGTG[C/G]GCAGTATCTTGCTGC | 179326 | | rs193622875 | snp | C/T | | | intron-variant | H24G06.1, ? | WS195 | V:9455920 | TTCAATCAGCCGCCT[C/T]CCCCAATCCTTTCGC | 179326 | |