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: rs6823767
rs6823767
4 150373933 intron variant T/C snv 0.28
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2018 2019
dbSNP: rs10010954
rs10010954
1.000 0.040 4 150324302 intron variant T/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs11936646
rs11936646
1.000 0.040 4 150427048 intron variant G/A snv 0.22
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs11945847
rs11945847
1.000 0.040 4 150350950 intron variant T/C snv 0.34
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs12499470
rs12499470
1.000 0.040 4 150400089 intron variant A/C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17504359
rs17504359
1.000 0.040 4 150385969 intron variant C/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17504366
rs17504366
1.000 0.040 4 150386061 intron variant A/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17504373
rs17504373
1.000 0.040 4 150386158 intron variant T/C snv 0.22
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17588356
rs17588356
4 150289525 intron variant G/T snv 0.19
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs2290846
rs2290846
1.000 0.040 4 150277928 missense variant G/A snv 0.20 0.18
CUI: C0242216
Disease: Biliary calculi
Biliary calculi
0.700 1.000 1 2018 2018
dbSNP: rs2290846
rs2290846
1.000 0.040 4 150277928 missense variant G/A snv 0.20 0.18
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs28521457
rs28521457
1.000 0.080 4 150759175 intron variant G/A;C snv
Chemical and Drug Induced Liver Injury
0.700 1.000 1 2017 2017
dbSNP: rs41386148
rs41386148
1.000 0.040 4 150399427 intron variant C/T snv 0.13
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs4370117
rs4370117
1.000 0.040 4 150416003 intron variant C/T snv 0.22
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs6535731
rs6535731
1.000 0.040 4 150346391 intron variant A/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs7657948
rs7657948
1.000 0.040 4 150363830 intron variant G/A snv 0.81
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs952097
rs952097
1.000 0.040 4 150395608 intron variant C/T snv 0.15
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017