Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3850641
rs3850641
TNFSF4
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.010 GeneticVariation BEFREE Furthermore, rs3850641 variant allele G was in strong association with hypothyroidism in Hashimoto's thyroiditis (HT) (p = 0.018). 27556446

2016