Disease: Waist-Hip Ratio
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10101067
EYA1
8 71495139 intron variant G/C snv 6.2E-02 2
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs1358980
LOC105375070
6 43796814 intergenic variant C/T snv 0.40 6
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs2207132 20 40513876 intergenic variant G/A snv 2.7E-02 4
rs2845885
FLRT1 ; MACROD1
11 64101590 intron variant C/T snv 0.87 5
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
rs4738141
EYA1
8 71557507 intron variant A/G snv 0.41 3
rs56271783
VEGFB
11 64237251 intron variant G/A;C;T snv 3.6E-05; 3.7E-02 2
rs605066 6 139508529 intron variant C/T snv 0.53 6
rs634869 6 139510620 intron variant T/A;C snv 5
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs72959041
RSPO3
6 127133748 intron variant G/A snv 3.2E-02 5
rs78058190 2 218835276 upstream gene variant G/A snv 3.9E-02 4
rs797486
DLEU7 ; DLEU1
13 50647482 intron variant C/A snv 0.85 2
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7
rs900399
LINC02029
3 157080943 upstream gene variant A/G snv 0.36 4
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs9991328
FAM13A
4 88791970 intron variant C/T snv 0.53 5
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45