Disease: Body mass index
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10795945 1.000 0.080 10 12260608 intergenic variant T/A;C snv 2
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 2
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 3
rs2246012
ARG1 ; MED23
1.000 0.080 6 131577068 intron variant T/A;C snv 2
rs2296172
MACF1
1.000 0.080 1 39370145 missense variant A/G;T snv 0.19; 8.0E-06 4
rs2299383
RELN
1.000 0.080 7 103778399 intron variant C/T snv 0.41 2
rs329122
JADE2 ; LOC107986451
1.000 0.080 5 134528909 intron variant G/A snv 0.45 2
rs35261542
CDKAL1
1.000 0.080 6 20675561 intron variant C/A snv 0.26 3
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 3
rs4865796
ARL15
1.000 0.080 5 53976834 intron variant G/A snv 0.72 3
rs6947395
AUTS2
1.000 0.080 7 69941675 intron variant A/T snv 0.20 2
rs7034200
GLIS3
1.000 0.080 9 4289050 intron variant C/A;G snv 3
rs7144011
NRXN3
1.000 0.080 14 79474040 intron variant G/T snv 0.21 4
rs72892910 1.000 0.080 6 50849174 downstream gene variant G/T snv 0.17 2
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs9891146
C17orf58
1.000 0.080 17 67991933 missense variant T/C snv 0.64 0.60 2
rs11671664
GIPR
0.925 0.120 19 45669020 intron variant G/A snv 0.12 2
rs11709077
PPARG
0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02 3
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 4
rs2307111
POC5
0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 5
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 5
rs7020996 0.925 0.120 9 22129580 downstream gene variant C/A;T snv 2
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 4