Disease: Waist-Hip Ratio
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10245353 7 25818994 intergenic variant C/A snv 0.16 4
rs10804591 3 129615390 intergenic variant C/A snv 0.63 5
rs10842707 12 26318431 intron variant C/G;T snv 4
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs10923712
TBX15
1 118962811 intron variant G/A snv 0.56 4
rs1106529
TBX15
1 118988874 intron variant G/A snv 0.77 3
rs12608504 19 18278325 upstream gene variant A/G;T snv 3
rs12692737
COBLL1
2 164697799 non coding transcript exon variant C/A snv 0.42 3
rs1294410
LOC101928004
6 6738519 intron variant T/C snv 0.65 3
rs1358980
LOC105375070
6 43796814 intergenic variant C/T snv 0.40 6
rs1385167
LOC105369168
2 65973514 intron variant A/G snv 0.18 3
rs1443512 12 53948900 downstream gene variant A/C;T snv 4
rs1534696
SNX10
7 26357619 intron variant C/A snv 0.58 3
rs1569135
LOC105373786
2 187250671 intron variant A/G snv 0.51 3
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs17819328 3 12447843 intergenic variant T/A;G snv 4
rs1936805
RSPO3
6 127130971 intron variant C/T snv 0.55 3
rs2276824
PBRM1
3 52603470 intron variant C/G snv 0.54 0.61 3
rs2294239
ZNRF3
22 29053489 intron variant A/G snv 0.36 4
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs2645294
WARS2
1 119031964 3 prime UTR variant C/T snv 0.59 4
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5
rs714515
DNM3 ; PIGC
1 172383850 intron variant G/A snv 0.46 3
rs7536458 1 118321979 intergenic variant T/G snv 0.23 5
rs7801581
HOXA11-AS ; HOXA11
7 27184152 intron variant C/T snv 0.24 5