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: rs10938397
rs10938397
0.851 0.200 4 45180510 intergenic variant A/G snv 0.37
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 14 2009 2019
dbSNP: rs543874
rs543874
1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 14 2010 2019
dbSNP: rs6567160
rs6567160
1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 12 2014 2019
dbSNP: rs7138803
rs7138803
0.827 0.240 12 49853685 intergenic variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 12 2009 2019
dbSNP: rs13107325
rs13107325
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 11 2010 2019
dbSNP: rs1558902
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 11 2010 2019
dbSNP: rs12429545
rs12429545
13 53528071 intron variant G/A;T snv 0.12
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 10 2015 2019
dbSNP: rs3810291
rs3810291
19 47065746 3 prime UTR variant G/A snv 0.50
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 10 2010 2019
dbSNP: rs2112347
rs2112347
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 9 2010 2019
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 1.000 9 2012 2019
dbSNP: rs10182181
rs10182181
1.000 0.080 2 24927427 intergenic variant A/G snv 0.57
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 8 2015 2019
dbSNP: rs13021737
rs13021737
2 632348 intergenic variant A/G snv 0.85
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 8 2015 2019
dbSNP: rs3817334
rs3817334
1.000 0.080 11 47629441 intron variant C/T snv 0.36
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 8 2010 2018
dbSNP: rs10132280
rs10132280
14 25458973 intergenic variant C/A snv 0.37
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2015 2019
dbSNP: rs12446632
rs12446632
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2015 2019
dbSNP: rs1516725
rs1516725
0.925 0.120 3 186106215 intron variant T/C snv 0.86
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2013 2019
dbSNP: rs17024393
rs17024393
1 109612066 intron variant T/C snv 4.6E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2015 2019
dbSNP: rs17405819
rs17405819
8 75894349 intergenic variant T/C snv 0.24
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2015 2019
dbSNP: rs1928295
rs1928295
9 117616205 intergenic variant T/C snv 0.45
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2015 2019
dbSNP: rs2365389
rs2365389
3 61250788 intron variant C/T snv 0.56
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2015 2018
dbSNP: rs3101336
rs3101336
1.000 0.080 1 72285502 intron variant T/C snv 0.62
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2015 2019
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2009 2019
dbSNP: rs6864049
rs6864049
5 124994829 intron variant A/C;G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2015 2019
dbSNP: rs9540493
rs9540493
1.000 0.040 13 65631572 intergenic variant A/G snv 0.49
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2015 2019
dbSNP: rs11030104
rs11030104
0.790 0.240 11 27662970 intron variant A/G snv 0.16
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 6 2014 2019