Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908866
rs121908866
TSHR ; LOC101928462
0.010 GeneticVariation BEFREE In conclusion, CH in the siblings is due to the missense mutation, W546X, in their TSHR gene. 12629076

2003