Have questions? Visit https://www.reddit.com/r/SNPedia

rs121907970(G;G)

From SNPedia
Miscall by Ancestry; actually represents the common/benign genotype
Is agenotype
ofrs121907970
GeneHEXA
Chromosome15
Position72,350,584
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 2 Carrier of a Tay-Sachs pseudodeficiency allele
(G;G) 0 Miscall by Ancestry; actually represents the common/benign genotype

Error by Ancestry; this should be the (C;C) common/benign genotype.