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rs61630004(A;A)

From SNPedia

significance unclear; slight change related to ectodermal dysplasia
Is agenotype
ofrs61630004
GeneKRT85
Chromosome12
Position52,367,173
mentionedby
Magnitude1
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