Talk:Rs104894422
From SNPedia
As per OMIM 608896.0002 the risk allele is A; patients with the related disease, Limb-Girdle Muscular Dystrophy type 2C, are either heterozygous or homozygous on the A allele. It is estimated 1 in 50 Romani carry the risk allele and there is an implied founder effect for it. In 23andMe, this SNP is i5000573.
