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: rs12134663
rs12134663
1 11778589 intron variant A/C;G snv
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement
0.800 1.000 1 2013 2013
dbSNP: rs12561919
rs12561919
1.000 0.040 1 11779866 missense variant C/T snv 0.13 0.13
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
0.700 1.000 1 2018 2018
dbSNP: rs12561919
rs12561919
1.000 0.040 1 11779866 missense variant C/T snv 0.13 0.13
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2018 2018
dbSNP: rs12561919
rs12561919
1.000 0.040 1 11779866 missense variant C/T snv 0.13 0.13
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2017 2017
dbSNP: rs137976953
rs137976953
1 11782952 intron variant T/- del 1.0E-01
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2019 2019
dbSNP: rs4846044
rs4846044
1 11779941 missense variant T/C;G snv 0.95
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs4846044
rs4846044
1 11779941 missense variant T/C;G snv 0.95
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
0.700 1.000 1 2018 2018
dbSNP: rs55738118
rs55738118
1 11778394 intron variant C/T snv 0.11
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs72640211
rs72640211
1 11778705 synonymous variant G/A snv 4.4E-02 4.8E-02
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
0.700 1.000 1 2018 2018