rs770374710(-;-)

common in clinvar

Is a	genotype
of	rs770374710
Gene	MAGEL2
Chromosome	15
Position	23,645,746
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;G)	9	Possible miscall in Ancestry v2c data; otherwise, Prader-Willi-like syndrome; Schaaf-Yang syndrome