Talk:Rs7755898
From SNPedia
This SNP is supposed to serve as a marker for the Q318X null allele of the 21-hydroxylase gene. This would generally be associated, when homozygous, with the most severe form of congenital adrenal hyperplasia (salt wasting). However, a random survey of 10 publicly uploaded genomes showed all 10 to be carriers. This is well out of Hardy-Weinberg equilibrium, making the accuracy of this SNP as reported by 23andme suspect. Positive results should be clinically correlated and verified in cooperation with your health care provider.
- CT is 93% of opensnp https://opensnp.org/snps/rs7755898#users so your observation holds. --- cariaso 01:38, 14 June 2015 (UTC)
