RAD51B, RAD51 paralog B, 5890

N. diseases: 126; N. variants: 108
Disease: Hypothyroidism ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3784099
rs3784099
Entrez Id: 5890
Gene Symbol: RAD51B
RAD51B
CUI: C0020676
Disease:
Hypothyroidism 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019