Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs368176907
rs368176907
TXNRD2
0.010 GeneticVariation BEFREE Previously, the p.R316C had only been found in severe RTH cases with homozygous mutations or with an ectopic thyroid. 25502991

2015