Disease: Waist-Hip Ratio
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 11
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 6
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs72959041
RSPO3
6 127133748 intron variant G/A snv 3.2E-02 5
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs605066 6 139508529 intron variant C/T snv 0.53 6
rs634869 6 139510620 intron variant T/A;C snv 5
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs900399
LINC02029
3 157080943 upstream gene variant A/G snv 0.36 4
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
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 5
rs3851294
DSTYK
1 205161285 missense variant A/G;T snv 0.93 2
rs78058190 2 218835276 upstream gene variant G/A snv 3.9E-02 4
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 6
rs4660808
PPIEL
1 39552837 intron variant C/T snv 0.17 3
rs2207132 20 40513876 intergenic variant G/A snv 2.7E-02 4
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11