rs121907970(G;G)
From SNPedia
Miscall by Ancestry; actually represents the common/benign genotype |
Is a | genotype |
of | rs121907970 |
Gene | HEXA |
Chromosome | 15 |
Position | 72,350,584 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(G;G) | 0 | Miscall by Ancestry; actually represents the common/benign genotype |
Error by Ancestry; this should be the (C;C) common/benign genotype.