Disease: Body mass index
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs6234
PCSK1 ; LOC101929710
0.851 0.160 5 96393270 missense variant G/C snv 0.27 0.24 4
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 3
rs10269783 7 49576607 intron variant G/A snv 0.36 2
rs2075803
SIGLEC9
1.000 0.040 19 51125272 missense variant A/G snv 0.55 0.52 2
rs2781668
ARG1 ; MED23
1.000 0.080 6 131576138 intron variant C/T snv 0.16 2
rs74447607 20 55872891 intergenic variant C/T snv 0.17 2