Source: ALL

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: rs35146602
rs35146602
4 145866089 intron variant A/G snv 0.15
Serum gamma-glutamyl transferase measurement
0.700 1.000 1 2019 2019
dbSNP: rs35879803
rs35879803
1.000 0.040 4 145861685 non coding transcript exon variant C/A;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2018 2018
dbSNP: rs4345206
rs4345206
1.000 0.040 4 145845384 intron variant T/C snv 0.59
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2018 2018
dbSNP: rs4835265
rs4835265
4 145900258 intron variant C/A snv 0.15
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs4835265
rs4835265
4 145900258 intron variant C/A snv 0.15
Aspartate aminotransferase measurement
0.700 1.000 1 2018 2018
dbSNP: rs4835265
rs4835265
4 145900258 intron variant C/A snv 0.15
Serum Alanine Aminotransferase Measurement
0.700 1.000 1 2018 2018
dbSNP: rs4835265
rs4835265
4 145900258 intron variant C/A snv 0.15
Gamma glutamyl transferase measurement
0.700 1.000 1 2011 2011
dbSNP: rs4835265
rs4835265
4 145900258 intron variant C/A snv 0.15
Alanine aminotransferase measurement
0.700 1.000 1 2018 2018
dbSNP: rs4835266
rs4835266
4 145900573 intron variant T/A;C snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs7666150
rs7666150
4 145893488 intron variant T/C snv 0.54
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2017 2017