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: rs12968116
rs12968116
ATP8B1 ; LOC100505549
18 57655270 missense variant C/T snv 8.2E-02 8.0E-02
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		0.800 1.000 1 2011 2011
dbSNP: rs12968116
rs12968116
ATP8B1 ; LOC100505549
18 57655270 missense variant C/T snv 8.2E-02 8.0E-02
CUI: C0242216
Disease: Biliary calculi
Biliary calculi 		0.700 1.000 1 2018 2018
dbSNP: rs17686020
rs17686020
ATP8B1 ; LOC100505549
1.000 0.040 18 57659569 intron variant A/G snv 0.11
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs17759233
rs17759233
ATP8B1 ; LOC100505549
1.000 0.040 18 57652212 intron variant G/A snv 0.12 7.9E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs17832328
rs17832328
ATP8B1 ; LOC100505549
1.000 0.040 18 57657967 intron variant G/A snv 7.9E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs17832346
rs17832346
ATP8B1 ; LOC100505549
1.000 0.040 18 57659538 intron variant G/A snv 9.5E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs17832364
rs17832364
ATP8B1 ; LOC100505549
1.000 0.040 18 57659616 intron variant C/T snv 7.9E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1893673
rs1893673
ATP8B1 ; LOC100505549
1.000 0.040 18 57660068 intron variant T/C snv 0.45
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs2663842
rs2663842
ATP8B1
18 57782284 intron variant G/A snv 0.70
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2019 2019
dbSNP: rs56950313
rs56950313
ATP8B1 ; LOC100505549
18 57658313 intron variant G/A snv 0.16
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs7226404
rs7226404
ATP8B1 ; LOC100505549
1.000 0.040 18 57652240 intron variant A/C snv 0.17
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs7239484
rs7239484
ATP8B1
0.925 0.040 18 57776480 intron variant C/A;T snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs7239484
rs7239484
ATP8B1
0.925 0.040 18 57776480 intron variant C/A;T snv
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018