rs387906553(A;G)
From SNPedia
Possible miscall in Ancestry v2 data; otherwise, severe congenital neutropenia, type 1, autosomal dominant |
Is a | genotype |
of | rs387906553 |
Gene | ELANE |
Chromosome | 19 |
Position | 853,022 |
mentioned | by |
Magnitude | 8.2 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(A;G) | 8.2 | Possible miscall in Ancestry v2 data; otherwise, severe congenital neutropenia, type 1, autosomal dominant |
(G;G) | 0 | common in clinvar |
see links at rs387906553