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: rs6738962
rs6738962
CTNNA2
1.000 0.080 2 80054047 intron variant A/G snv 7.9E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.800 1.000 1 2014 2014
dbSNP: rs10196867
rs10196867
CTNNA2
0.925 0.080 2 79751234 intron variant C/G;T snv
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.710 1.000 1 2019 2019
dbSNP: rs17016673
rs17016673
CTNNA2 ; LOC105374823 ; LOC107985902
2 79270653 intron variant C/G snv 0.14
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2015 2018
dbSNP: rs10180106
rs10180106
CTNNA2
1.000 0.040 2 79994772 intron variant G/A snv 0.22
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2018 2018
dbSNP: rs10196867
rs10196867
CTNNA2
0.925 0.080 2 79751234 intron variant C/G;T snv
CUI: C0019337
Disease: Heroin Dependence
Heroin Dependence 		0.700 1.000 1 2019 2019
dbSNP: rs10196867
rs10196867
CTNNA2
0.925 0.080 2 79751234 intron variant C/G;T snv
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		0.700 1.000 1 2019 2019
dbSNP: rs10196867
rs10196867
CTNNA2
0.925 0.080 2 79751234 intron variant C/G;T snv
CUI: C0236733
Disease: Amphetamine-Related Disorders
Amphetamine-Related Disorders 		0.700 1.000 1 2019 2019
dbSNP: rs10196867
rs10196867
CTNNA2
0.925 0.080 2 79751234 intron variant C/G;T snv
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		0.700 1.000 1 2019 2019
dbSNP: rs1031442
rs1031442
CTNNA2
1.000 0.040 2 80105025 intron variant T/C snv 0.22
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs11685451
rs11685451
CTNNA2
1.000 0.040 2 80138067 intron variant C/T snv 0.23
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs11685504
rs11685504
CTNNA2
1.000 0.040 2 80138168 intron variant C/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs11695685
rs11695685
CTNNA2
2 79695676 intron variant C/T snv 0.29
CUI: C2697758
Disease: Interleukin 10 Measurement
Interleukin 10 Measurement 		0.700 1.000 1 2008 2008
dbSNP: rs12472249
rs12472249
CTNNA2
1.000 0.040 2 80102954 intron variant C/T snv 6.9E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs13025833
rs13025833
CTNNA2
1.000 0.080 2 79716982 intron variant A/G snv 0.43
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2015 2015
dbSNP: rs1348557
rs1348557
CTNNA2
2 80420752 intron variant A/G snv 0.15
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs1864548
rs1864548
CTNNA2
1.000 0.040 2 79462446 intron variant T/C snv 0.33
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1864550
rs1864550
CTNNA2
1.000 0.040 2 79472456 intron variant T/C snv 0.31
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs2250249
rs2250249
CTNNA2
1.000 0.040 2 79471870 intron variant G/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs2862025
rs2862025
CTNNA2
2 80257468 intron variant C/G snv 0.17
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs2916490
rs2916490
CTNNA2
2 79965226 intron variant G/A snv 0.25
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs3849389
rs3849389
CTNNA2
1.000 0.040 2 80132127 intron variant G/A snv 0.37
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs445551
rs445551
CTNNA2
1.000 0.040 2 79470856 intron variant G/A;T snv 0.36
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs4852146
rs4852146
CTNNA2
2 79397862 intron variant C/T snv 0.71
CUI: C0042879
Disease: Vitamin K Assay
Vitamin K Assay 		0.700 1.000 1 2014 2014
dbSNP: rs563702
rs563702
CTNNA2
1.000 0.040 2 79999656 intron variant T/C snv 0.18
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs6752828
rs6752828
CTNNA2
2 79960843 intron variant C/T snv 0.48
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2015 2015