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: rs13088462
rs13088462
DOCK3
3 51034282 intron variant T/C;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2010 2014
dbSNP: rs73072483
rs73072483
DOCK3
3 50734193 intron variant G/A snv 9.6E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs10510754
rs10510754
DOCK3
1.000 0.040 3 50824180 intron variant A/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs10510757
rs10510757
DOCK3
3 51372633 intron variant C/G snv 6.6E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs11130263
rs11130263
DOCK3
1.000 0.040 3 50894893 intron variant G/A snv 0.16
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs11917538
rs11917538
DOCK3
1.000 0.040 3 50835545 intron variant G/A snv 0.77
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs11920441
rs11920441
DOCK3
3 51062589 intron variant T/C snv 0.26
CUI: C4317009
Disease: Diverticular Diseases
Diverticular Diseases 		0.700 1.000 1 2018 2018
dbSNP: rs11921930
rs11921930
DOCK3
1.000 0.040 3 50859955 intron variant G/A snv 0.15
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs13069365
rs13069365
DOCK3
3 50979528 intron variant G/A;T snv
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		0.700 1.000 1 2019 2019
dbSNP: rs1552074
rs1552074
DOCK3
3 51370620 intron variant C/T snv 0.88
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs17659990
rs17659990
DOCK3
0.790 0.080 3 50713718 intron variant C/T snv 2.1E-02
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2017 2017
dbSNP: rs17659990
rs17659990
DOCK3
0.790 0.080 3 50713718 intron variant C/T snv 2.1E-02
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2017 2017
dbSNP: rs17659990
rs17659990
DOCK3
0.790 0.080 3 50713718 intron variant C/T snv 2.1E-02
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2017 2017
dbSNP: rs17659990
rs17659990
DOCK3
0.790 0.080 3 50713718 intron variant C/T snv 2.1E-02
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2017 2017
dbSNP: rs17659990
rs17659990
DOCK3
0.790 0.080 3 50713718 intron variant C/T snv 2.1E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs17659990
rs17659990
DOCK3
0.790 0.080 3 50713718 intron variant C/T snv 2.1E-02
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2017 2017
dbSNP: rs17659990
rs17659990
DOCK3
0.790 0.080 3 50713718 intron variant C/T snv 2.1E-02
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2017 2017
dbSNP: rs17659990
rs17659990
DOCK3
0.790 0.080 3 50713718 intron variant C/T snv 2.1E-02
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2017 2017
dbSNP: rs17659990
rs17659990
DOCK3
0.790 0.080 3 50713718 intron variant C/T snv 2.1E-02
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2017 2017
dbSNP: rs1947607
rs1947607
DOCK3
1.000 0.040 3 50813669 intron variant T/C snv 9.5E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs2219431
rs2219431
DOCK3
1.000 0.040 3 50837715 intron variant G/T snv 9.9E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs2609031
rs2609031
DOCK3
1.000 0.040 3 50820365 intron variant C/T snv 9.5E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs2675806
rs2675806
DOCK3 ; ZNF652P1
1.000 0.040 3 50786798 non coding transcript exon variant C/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs2675810
rs2675810
DOCK3
1.000 0.040 3 50751155 intron variant G/C snv 9.5E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs2675830
rs2675830
DOCK3
1.000 0.040 3 50819337 intron variant C/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017