| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193339328 | snp | G/T | 0.0198 | 0.0975088 | synonymous-codon | daf-15 | WS195 | IV:9390314 | TGTTGAAGAAACTGT[G/T]CATGAAGACGGAATA | 177770 |
| rs193339329 | snp | C/T | 0.019998 | 0.0979748 | intron-variant | daf-15 | WS195 | IV:9392582 | ATTTTCCTCGATTTT[C/T]TTAGTTTTTCTCTCG | 177770 |
| rs193339330 | snp | C/T | 0.0200984 | 0.0982103 | intron-variant | daf-15 | WS195 | IV:9392583 | TTTTCCTCGATTTTT[C/T]TAGTTTTTCTCTCGT | 177770 |
| rs193339331 | snp | A/C | 0.019998 | 0.0979748 | intron-variant | daf-15 | WS195 | IV:9392585 | TTCCTCGATTTTTTT[A/C]GTTTTTCTCTCGTGG | 177770 |
| rs193339332 | snp | C/T | 0.019998 | 0.0979748 | intron-variant | daf-15 | WS195 | IV:9392592 | ATTTTTTTAGTTTTT[C/T]TCTCGTGGTATTACT | 177770 |
| rs193339333 | snp | A/G | 0.01005 | 0.0701712 | intron-variant | daf-15 | WS195 | IV:9392616 | TATTACTGAAATTAA[A/G]AATATTTTTGGTTTT | 177770 |
| rs193608708 | snp | A/G | | | intron-variant | daf-15 | WS195 | IV:9386748 | ACGAAAAAAAAAACA[A/G]CAAATTAATGGAAAA | 177770 |
| rs193929495 | snp | C/T | | | missense | daf-15 | WS195 | IV:9388319 | TCAACTGGATATTCA[C/T]TGCCATCACTGACAC | 177770 |