Source: GWASCAT

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: rs1239948
rs1239948
13 50532386 intron variant A/T snv 0.59
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs1239948
rs1239948
13 50532386 intron variant A/T snv 0.59
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs1239948
rs1239948
13 50532386 intron variant A/T snv 0.59
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2017 2017