Links to SNPedia
Note: For some SNPs, testing providers detect the genotype from the opposite strand of DNA, so that the genotypes listed on openSNP don't appear here. In those cases, please replace "A" by "T" or "G" by "C" (and vice-versa).
Publications on this SNP on the Public Library of Science:
There are no PLoS-results yet. Please come back again later.
Publications on this SNP on Mendeley
There are no Mendeley results yet. Please come back again later.
Evidence compiled by the Personal Genome Project
||Low clinical importance, Likely benign
||This variant has a 3.5% allele frequency in 1000 genomes data. Although OMIM links this to disease, the paper they reference uses in vitro data to conclude that this is a functionally neutral polymorphism.
Publications listed by Genome.gov
There are no results from genome.gov yet. Please come back later.
Users who share this SNP: