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rs770374710(-;G)

From SNPedia
Possible miscall in Ancestry v2c data; otherwise, Prader-Willi-like syndrome; Schaaf-Yang syndrome
Is agenotype
ofrs770374710
GeneMAGEL2
Chromosome15
Position23,645,746
mentionedby
Magnitude9
ReputeBad
Geno Mag Summary
(-;-) 0 common in clinvar
(-;G) 9 Possible miscall in Ancestry v2c data; otherwise, Prader-Willi-like syndrome; Schaaf-Yang syndrome

see discussion at MAGEL2