Disease: Waist Circumference
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 7
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 7
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs7133378
DNAH10 ; CCDC92
12 123924955 intron variant G/A snv 0.38 6
rs2650492
SBK1
16 28322090 3 prime UTR variant G/A snv 0.20 5
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 5
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 5
rs12429545 13 53528071 intron variant G/A;T snv 0.12 4
rs12885454
LOC102724934
14 29267632 non coding transcript exon variant C/A snv 0.27 4
rs2033529
TDRG1
6 40380914 intron variant A/C;G snv 4
rs806794
H2AC7 ; H3C4 ; H2BC7
6 26200449 3 prime UTR variant A/G snv 0.36 4
rs7550711
GPR61
1 109540264 intron variant C/T snv 2.6E-02 3
rs943005 6 50898107 non coding transcript exon variant C/T snv 0.16 3