Disease: Waist-Hip Ratio
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 7
rs2145272 20 6645571 intergenic variant G/A;T snv 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs1358980
LOC105375070
6 43796814 intergenic variant C/T snv 0.40 6
rs7133378
DNAH10 ; CCDC92
12 123924955 intron variant G/A snv 0.38 6
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 5
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 5
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 5
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5
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
rs979012 1.000 0.080 20 6642727 intergenic variant T/C snv 0.67 5
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 5
rs10804591 3 129615390 intergenic variant C/A snv 0.63 4
rs10842707 12 26318431 intron variant C/G;T snv 4