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rs121918166(A;G)

From SNPedia
Carrier of an oculocutaneous Albinism Type II mutation
Is agenotype
ofrs121918166
GeneOCA2
Chromosome15
Position27,985,101
Merged fromRs28934272
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;G) 3 Carrier of an oculocutaneous Albinism Type II mutation
(G;G) 0 common in clinvar

Unaffected unless carrying another pathogenic OCA2 gene mutation