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
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 7
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 6
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 8
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 9
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
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
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
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
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
rs4660808
PPIEL
1 39552837 intron variant C/T snv 0.17 3
rs4738141
EYA1
8 71557507 intron variant A/G snv 0.41 3
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