Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1012657750
rs1012657750
SELENBP1
1 151368294 missense variant G/C snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2020 2020
dbSNP: rs1012657750
rs1012657750
SELENBP1
1 151368294 missense variant G/C snv
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		0.010 1.000 1 2020 2020