Disease: Waist-Hip Ratio
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C 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
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 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
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 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
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 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
rs905938
ZBTB7B ; DCST2
1 155018913 intron variant T/C snv 0.24 5