RAD51B, RAD51 paralog B, 5890

N. diseases: 126; N. variants: 108
Disease: Hypothyroidism ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3784099
rs3784099 		0.807 0.320 14 68283210 intron variant G/A snv 0.43
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		Endocrine System Diseases 0.700 1.000 1 2019 2019