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
Gene |
Impact |
Trait |
Summary |
Inheritance |
MYO7A |
High clinical importance, Uncertain pathogenic |
|
May cause Usher Type I syndrome in a recessive manner (congenital deafness and loss of vision in childhood), but reports are conflicting and there is no statistical significance in published observations. |
recessive |
Publications listed by Genome.gov
There are no results from genome.gov yet. Please come back later.
Users who share this SNP: