Disease: Hip 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
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
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 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
rs17024393
GNAT2
1 109612066 intron variant T/C snv 4.6E-02 4
rs806794
H2AC7 ; H3C4 ; H2BC7
6 26200449 3 prime UTR variant A/G snv 0.36 4
rs11672660
GIPR ; MIR642B
19 45676926 intron variant C/T snv 0.18 0.17 3
rs3800229
FOXO3
1.000 0.040 6 108675760 intron variant G/T snv 0.54 3
rs1294409
LOC101928004
6 6738122 intron variant C/T snv 0.63 2
rs7632381
ZBTB38
3 141387221 non coding transcript exon variant T/A;C snv 2