Disease: Waist-Hip Ratio
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7536458 1 118321979 intergenic variant T/G snv 0.23 5
rs10923712
TBX15
1 118962811 intron variant G/A snv 0.56 4
rs1106529
TBX15
1 118988874 intron variant G/A snv 0.77 3
rs2645294
WARS2
1 119031964 3 prime UTR variant C/T snv 0.59 4
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 6
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7
rs17819328 3 12447843 intergenic variant T/A;G snv 4
rs1936805
RSPO3
6 127130971 intron variant C/T snv 0.55 3
rs10804591 3 129615390 intergenic variant C/A snv 0.63 5
rs905938
ZBTB7B ; DCST2
1 155018913 intron variant T/C snv 0.24 5
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 7
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs12692737
COBLL1
2 164697799 non coding transcript exon variant C/A snv 0.42 3
rs9435732
MFAP2
1 16981663 intron variant C/G;T snv 4
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs714515
DNM3 ; PIGC
1 172383850 intron variant G/A snv 0.46 3
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5
rs12608504 19 18278325 upstream gene variant A/G;T snv 3
rs1569135
LOC105373786
2 187250671 intron variant A/G snv 0.51 3
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs10245353 7 25818994 intergenic variant C/A snv 0.16 4
rs10842707 12 26318431 intron variant C/G;T snv 4
rs1534696
SNX10
7 26357619 intron variant C/A snv 0.58 3
rs7801581
HOXA11-AS ; HOXA11
7 27184152 intron variant C/T snv 0.24 5