Disease: Waist-Hip Ratio
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
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
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs3741378
SIPA1
0.851 0.080 11 65641466 missense variant C/G;T snv 0.15 8
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 7
rs2067087
HOTTIP ; HOXA13
1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 6
rs1250259
FN1 ; LOC105373868
1.000 0.040 2 215435759 missense variant T/A snv 0.76 0.79 5
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 5
rs7246865
MYO9B
19 17108295 intron variant G/A snv 0.36 5
rs8126001
RGS19 ; OPRL1
20 64080106 5 prime UTR variant C/T snv 0.46 4
rs9844972 1.000 0.080 3 150379848 regulatory region variant G/A;C snv 4
rs936226 15 74776941 intergenic variant C/T snv 0.69 3
rs10788569
CFL1P1
10 87844975 non coding transcript exon variant T/C snv 0.23 2
rs2745599
FOXC1
6 1613451 3 prime UTR variant A/G;T snv 2
rs6090040
TCEA2
20 64060707 intron variant A/C snv 0.52 2