Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908873
rs121908873
TSHR ; LOC101928462
0.010 GeneticVariation BEFREE This is consistent with the finding that only the index patient with the additional somatic mutation S281N was hyperthyroid. 18466076

2008