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: rs4855074
rs4855074
1.000 0.080 3 179450674 intron variant C/T snv 0.13
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.700 1.000 1 2018 2018
dbSNP: rs4855075
rs4855075
1.000 0.080 3 179452706 upstream gene variant C/T snv 0.13
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.700 1.000 1 2018 2018
dbSNP: rs7611674
rs7611674
3 179451442 5 prime UTR variant T/G snv 0.27
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2018 2018