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From SNPedia

OMIM 601771.0008 indicates that the risk allele is A, but only homozygously, for Primary Congenital Glaucoma 3 A. Of the 43 patients tested with this disease, from a total of 26 Slovak Rom familes, all were homozygous for this SNP. I may be reading it wrong, but it appears that a study of 21 Bulgarian Roma from 16 different families showed 5 different mutations, saying it is inconclusive for this group. In 23andMe, this SNP is i3003542.