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
0.846 0.179 4 45180510 intergenic variant A/G snp 0.38
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 9 2009 2017
dbSNP: rs543874
rs543874
1.000 0.071 1 177920345 regulatory region variant A/G snp 0.20
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 9 2010 2017
dbSNP: rs7138803
rs7138803
0.923 0.107 12 49853685 intergenic variant G/A,T snp 0.32; 3.2E-05
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 8 2009 2017
dbSNP: rs1558902
rs1558902
FTO
0.846 0.071 16 53769662 intron variant T/A snp 0.32
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 7 2010 2017
dbSNP: rs6567160
rs6567160
1.000 0.071 18 60161902 T/C snp 0.20
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 6 2012 2017
dbSNP: rs13107325
rs13107325
1.000 0.036 4 102267552 missense variant C/A,T snp 4.0E-06; 4.5E-02 4.3E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 5 2010 2017
dbSNP: rs2112347
rs2112347
1.000 0.071 5 75719417 intergenic variant T/G snp 0.43
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 5 2010 2017
dbSNP: rs29941
rs29941
0.878 0.143 19 33818627 intergenic variant A/G snp 0.69
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 5 2009 2017
dbSNP: rs3810291
rs3810291
19 47065746 3 prime UTR variant G/A snp 0.50
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 5 2010 2017
dbSNP: rs3817334
rs3817334
1.000 0.071 11 47629441 intron variant C/T snp 0.36
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 5 2010 2017
dbSNP: rs11671664
rs11671664
0.923 0.107 19 45669020 intron variant G/A snp 0.13
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 4 2012 2017
dbSNP: rs1516725
rs1516725
1.000 0.071 3 186106215 intron variant T/C snp 0.87
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 4 2013 2017
dbSNP: rs8050136
rs8050136
FTO
0.744 0.321 16 53782363 intron variant C/A snp 0.40
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 4 2009 2017
dbSNP: rs987237
rs987237
1.000 0.071 6 50835337 intron variant A/G snp 0.18
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 4 2010 2017
dbSNP: rs9939609
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 4 2007 2016
dbSNP: rs10968576
rs10968576
1.000 0.071 9 28414341 intron variant A/G snp 0.28
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 3 2010 2017
dbSNP: rs11030104
rs11030104
0.878 0.071 11 27662970 intron variant A/G snp 0.16
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 3 2015 2017
dbSNP: rs13130484
rs13130484
1.000 0.071 4 45173674 intergenic variant C/A,T snp 3.2E-05; 0.37
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 3 2014 2017
dbSNP: rs17782313
rs17782313
0.734 0.250 18 60183864 intergenic variant T/C snp 0.23
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 3 2008 2017
dbSNP: rs2030323
rs2030323
1.000 0.071 11 27706992 intron variant A/C snp 0.83
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 3 2012 2017
dbSNP: rs2287019
rs2287019
1.000 0.071 19 45698914 intron variant C/T snp 0.17 0.18
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 3 2010 2017
dbSNP: rs4776970
rs4776970
15 67788548 intron variant A/T snp 0.43
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 3 2012 2017
dbSNP: rs571312
rs571312
1.000 0.071 18 60172536 intergenic variant C/A snp 0.25
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 3 2010 2017
dbSNP: rs633715
rs633715
1.000 0.071 1 177883445 intergenic variant T/C snp 0.17
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 3 2013 2017
dbSNP: rs7647305
rs7647305
3 186116501 intron variant T/C snp 0.75
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 3 2009 2017