rs61630004(A;A)
From SNPedia
significance unclear; slight change related to ectodermal dysplasia |
Is a | genotype |
of | rs61630004 |
Gene | KRT85 |
Chromosome | 12 |
Position | 52,367,173 |
mentioned | by |
Magnitude | 1 |
Geno | Mag | Summary |
---|---|---|
(A;A) | 1 | significance unclear; slight change related to ectodermal dysplasia |
(A;G) | 1 | significance unclear; possibly a carrier for an ectodermal dysplasia allele |
(G;G) | 0 | common in clinvar |
see discussion at rs61630004