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: rs8182584
rs8182584
19 33418804 intron variant T/C;G snv
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
0.700 1.000 1 2012 2012
dbSNP: rs8182584
rs8182584
19 33418804 intron variant T/C;G snv
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
0.700 1.000 1 2012 2012
dbSNP: rs889138
rs889138
19 33401503 intron variant C/T snv 0.53
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs889138
rs889138
19 33401503 intron variant C/T snv 0.53
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs889140
rs889140
19 33398094 intron variant G/A;C snv
CUI: C2700366
Disease: Adiponectin Measurement
Adiponectin Measurement
0.800 1.000 1 2014 2014
dbSNP: rs3786897
rs3786897
1.000 0.080 19 33402102 intron variant A/G snv 0.45
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 3 2015 2019
dbSNP: rs10406327
rs10406327
1.000 0.080 19 33399932 intron variant C/G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10406327
rs10406327
1.000 0.080 19 33399932 intron variant C/G;T snv
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 1 2019 2019
dbSNP: rs10425465
rs10425465
1.000 0.040 19 33407028 intron variant T/G snv 0.34
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2015 2015
dbSNP: rs3786897
rs3786897
1.000 0.080 19 33402102 intron variant A/G snv 0.45
Diabetes Mellitus, Non-Insulin-Dependent
0.820 0.667 1 2011 2019
dbSNP: rs3786897
rs3786897
1.000 0.080 19 33402102 intron variant A/G snv 0.45
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2017 2017
dbSNP: rs3786897
rs3786897
1.000 0.080 19 33402102 intron variant A/G snv 0.45
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
0.700 1.000 1 2017 2017
dbSNP: rs3786897
rs3786897
1.000 0.080 19 33402102 intron variant A/G snv 0.45
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017