rs764196809(CTCC;CTCC)
From SNPedia
common in clinvar |
Is a | genotype |
of | rs764196809 |
Gene | UNC13D |
Chromosome | 17 |
Position | 75,834,093 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
Geno | Mag | Summary |
---|---|---|
(-;CTCC) | 3 | Carrier of a hemophagocytic lymphohistiocytosis (HLH) mutation |
(CTCC;CTCC) | 0 | common in clinvar |
(I;I) | 0 | common genotype |