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: rs9991259
rs9991259
4 111765198 intergenic variant G/A snv 0.56
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs998584
rs998584
6 43790159 downstream gene variant C/A snv 0.41
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2015 2019
dbSNP: rs9983113
rs9983113
21 38943392 intron variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs9973932
rs9973932
2 207385798 intron variant T/G snv 0.17
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs9971845
rs9971845
12 33225563 intergenic variant T/C;G snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs9965170
rs9965170
18 47261903 upstream gene variant G/A;C;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs9956644
rs9956644
DCC
18 52867330 intron variant T/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs9955276
rs9955276
18 1839338 intron variant C/T snv 0.22
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs9953924
rs9953924
18 26680575 intron variant C/G snv 0.92
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs995258
rs995258
1 96965496 regulatory region variant A/C snv 0.34
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs9951893
rs9951893
18 63072017 regulatory region variant T/C snv 0.57
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs9944807
rs9944807
18 47262537 upstream gene variant A/G snv 0.37
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs9944545
rs9944545
18 60291011 upstream gene variant C/T snv 0.35
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2018 2018
dbSNP: rs9944241
rs9944241
15 51605861 intron variant T/C snv 2.9E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs994270
rs994270
6 51322989 intergenic variant C/A;G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs9942416
rs9942416
5 75741470 intergenic variant C/G snv 0.53
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2016 2016
dbSNP: rs9941349
rs9941349
FTO
1.000 0.080 16 53791576 intron variant C/T snv 0.34
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2017 2019
dbSNP: rs9940128
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2013 2019
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 6 2007 2019
dbSNP: rs9937053
rs9937053
FTO
0.882 0.160 16 53765595 intron variant G/A snv 0.42
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs9936385
rs9936385
FTO
0.925 0.120 16 53785257 intron variant T/C snv 0.41
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2015 2015
dbSNP: rs9932690
rs9932690
16 64684245 intergenic variant C/T snv 0.48
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs9930506
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2007 2019
dbSNP: rs9930333
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs9930024
rs9930024
16 67297951 intron variant T/C snv 0.56
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017