Disease: Waist-Hip Ratio
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 9
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 6
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 5
rs9844972 1.000 0.080 3 150379848 regulatory region variant G/A;C snv 4
rs35169799
PLCB3
0.925 0.200 11 64263769 missense variant C/T snv 4.9E-02 4.5E-02 3
rs3764002
LOC105369965 ; WSCD2
1.000 0.080 12 108224853 missense variant C/T snv 0.27 0.20 3
rs10260148
LOC105375508
1.000 0.080 7 130746210 intergenic variant C/T snv 0.27 2
rs622217 1.000 0.080 6 160345738 upstream gene variant T/A;C snv 2
rs757110
ABCC8
0.851 0.080 11 17396930 missense variant C/A;T snv 0.64; 8.0E-06 2
rs9369425
LOC107986598
0.882 0.160 6 43843237 downstream gene variant G/A snv 0.66 2