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From SNPedia

The first paragraph states that the risk allele for this SNP is rs1208(G). However in the ClinVar table on the right column, it shows Risk Rs1208(A;A).

Should the ClinVar risk genotype be modified to Risk Rs1208(G;G)??


This is likely to be a case of which phenotype should be considered riskier, or, normal? Both alleles are quite common. But we'll look into this a bit more and then reply further.Greg (talk) 18:03, 20 April 2017 (UTC)