i5012660
From SNPedia
| 23andMe data | I5012660 |
| 23andMe search | I5012660 |
| opensnp | I5012660 |
| Gene (via rs) | BCS1L, ZNF142 |
| iGeno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | normal |
| (A;G) | 4 | Gracile Syndrome carrier |
| (G;G) | 5 | Gracile Syndrome |
| alias | rs28937590 |
| Rs_StabilizedOrientation | plus |
| RsGeno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| (A;G) | 3 | carrier for a GRACILE syndrome mutation |
| (G;G) | 8 | GRACILE syndrome |
GRACILE syndrome is a very rare metabolic disorder that affects newborn infants of Finnish ancestry.
