Autosomal Dominant Robinow Syndrome 1
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Associated Variants (28)
| RSID | Gene | Evidence |
|---|---|---|
| RS1553677967 | WNT5A | strong |
| RS755916316 | WNT5A | strong |
| RS2106955417 | WNT5A | strong |
| RS554762368 | WNT5A | strong |
| RS369701725 | WNT5A | strong |
| RS786204837 | WNT5A | strong |
| RS780909370 | DVL1 | strong |
| RS2144572390 | FZD2 | strong |
| RS2106946273 | WNT5A | strong |
| RS1643642110 | DVL1 | strong |
| RS142925511 | DVL1 | strong |
| RS1568105666 | FZD2 | strong |
| RS1223920489 | FZD2 | strong |
| RS1553677971 | WNT5A | strong |
| RS387906663 | WNT5A | strong |
| RS869025219 | DVL3 | strong |
| RS869025218 | DVL3 | strong |
| RS869025217 | DVL3 | strong |
| RS869025216 | DVL3 | strong |
| RS869025215 | DVL3 | strong |
| RS797044839 | DVL1 | strong |
| RS786204836 | WNT5A | strong |
| RS139616809 | WNT5A | strong |
| RS181894008 | WNT5A | strong |
| RS188798140 | WNT5A | strong |
| RS6790979 | WNT5A | strong |
| RS587784562 | WNT5A | strong |
| RS786200925 | WNT5A | strong |