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: rs13253386
rs13253386
8 14144511 intron variant T/G snv 0.38
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 2 2018 2018
dbSNP: rs6990042
rs6990042
8 14316465 intron variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2015 2015
dbSNP: rs10088748
rs10088748
1.000 0.120 8 14611016 intron variant C/A snv 0.51
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2019 2019
dbSNP: rs10106919
rs10106919
1.000 0.040 8 14516676 intron variant A/C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs10216809
rs10216809
0.925 0.080 8 14507414 intron variant C/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs10503499
rs10503499
1.000 0.040 8 14527828 intron variant G/C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs115706913
rs115706913
8 14224308 intron variant T/C snv 2.7E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2017 2017
dbSNP: rs12155874
rs12155874
8 14098279 intron variant A/G snv 0.35
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 1 2019 2019
dbSNP: rs12547159
rs12547159
1.000 0.040 8 14994293 intron variant G/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs12675921
rs12675921
8 14131980 intron variant G/A snv 0.17
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 1 2018 2018
dbSNP: rs12682628
rs12682628
8 14111223 intron variant T/C snv 0.43
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 1 2018 2018
dbSNP: rs13259015
rs13259015
1.000 0.040 8 14520394 intron variant G/A snv 0.37
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs13263601
rs13263601
8 14238391 intron variant A/C snv 0.28
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs13278000
rs13278000
1.000 0.040 8 14995175 intron variant A/C;G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs1381410
rs1381410
1.000 0.040 8 14527811 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: rs17119539
rs17119539
1.000 0.040 8 14516481 intron variant G/A snv 7.4E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17119601
rs17119601
1.000 0.040 8 14518586 intron variant G/T snv 0.63
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17119607
rs17119607
1.000 0.040 8 14519772 intron variant T/C snv 4.4E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17119609
rs17119609
1.000 0.040 8 14519883 intron variant A/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17119646
rs17119646
1.000 0.040 8 14526528 intron variant T/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17119650
rs17119650
1.000 0.040 8 14526767 intron variant G/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17120351
rs17120351
0.925 0.040 8 14829488 intron variant T/C snv 2.7E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
0.700 1.000 1 2018 2018
dbSNP: rs17120351
rs17120351
0.925 0.040 8 14829488 intron variant T/C snv 2.7E-02
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs17608413
rs17608413
8 14953660 intron variant C/A;G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs17608649
rs17608649
1.000 0.040 8 14995579 intron variant C/G snv 0.18
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017