Disease: Waist-Hip Ratio
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs4738141
EYA1
8 71557507 intron variant A/G snv 0.41 3
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 6
rs900399
LINC02029
3 157080943 upstream gene variant A/G snv 0.36 4
rs3851294
DSTYK
1 205161285 missense variant A/G;T snv 0.93 2
rs797486
DLEU7 ; DLEU1
13 50647482 intron variant C/A snv 0.85 2
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 6
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 9
rs1358980
LOC105375070
6 43796814 intergenic variant C/T snv 0.40 6
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 5
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 11
rs2845885
FLRT1 ; MACROD1
11 64101590 intron variant C/T snv 0.87 5
rs4660808
PPIEL
1 39552837 intron variant C/T snv 0.17 3
rs605066 6 139508529 intron variant C/T snv 0.53 6
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7
rs9991328
FAM13A
4 88791970 intron variant C/T snv 0.53 5
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 8
rs112875651 8 125494452 intron variant G/A snv 0.31 7