Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3776070
rs3776070
SLC26A2
0.010 GeneticVariation BEFREE The homozygous A2092T (T689S) mutation could be one of the mutations in the DTDST gene causing MED. 23934641

2014