Disease: Waist-Hip Ratio
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4
rs3851294
DSTYK
1 205161285 missense variant A/G;T snv 0.93 2
rs4660808
PPIEL
1 39552837 intron variant C/T snv 0.17 3
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 7
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 9
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 8
rs78058190 2 218835276 upstream gene variant G/A snv 3.9E-02 4
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs900399
LINC02029
3 157080943 upstream gene variant A/G snv 0.36 4
rs9991328
FAM13A
4 88791970 intron variant C/T snv 0.53 5
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 6
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs1358980
LOC105375070
6 43796814 intergenic variant C/T snv 0.40 6
rs605066 6 139508529 intron variant C/T snv 0.53 6
rs634869 6 139510620 intron variant T/A;C snv 5
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs72959041
RSPO3
6 127133748 intron variant G/A snv 3.2E-02 5
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 8
rs10101067
EYA1
8 71495139 intron variant G/C snv 6.2E-02 2
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 5