Source: GWASDB

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: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 1.000 1 2012 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 1 2012 2019
dbSNP: rs7944584
rs7944584
1.000 0.080 11 47314769 intron variant A/T snv 0.19
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 1.000 1 2012 2012
dbSNP: rs8050136
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 1.000 1 2009 2019