Disease: Waist-Hip Ratio
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9991328
FAM13A
4 88791970 intron variant C/T snv 0.53 5
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 11
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 8
rs4738141
EYA1
8 71557507 intron variant A/G snv 0.41 3
rs10101067
EYA1
8 71495139 intron variant G/C snv 6.2E-02 2
rs56271783
VEGFB
11 64237251 intron variant G/A;C;T snv 3.6E-05; 3.7E-02 2
rs2845885
FLRT1 ; MACROD1
11 64101590 intron variant C/T snv 0.87 5
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 9
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs797486
DLEU7 ; DLEU1
13 50647482 intron variant C/A snv 0.85 2
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
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
rs1358980
LOC105375070
6 43796814 intergenic variant C/T snv 0.40 6
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs2207132 20 40513876 intergenic variant G/A snv 2.7E-02 4
rs4660808
PPIEL
1 39552837 intron variant C/T snv 0.17 3
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 6
rs78058190 2 218835276 upstream gene variant G/A snv 3.9E-02 4
rs3851294
DSTYK
1 205161285 missense variant A/G;T snv 0.93 2
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 5