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rs121907981(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs121907981
GeneHEXA
Chromosome15
Position72,345,550
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 8.8 Tay-Sachs disease (predicted)
(C;G) 3 Carrier of a Tay-Sachs mutation
(G;G) 0 common in clinvar