Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 13
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs11205303
MTMR11
0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 8
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 7
rs35874463
SMAD3
0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02 7
rs13241427 1.000 7 1249003 regulatory region variant G/T snv 0.72 6
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs72755233
ADAMTS17
1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 5
rs1993976
LINC02251
1.000 15 98063084 intron variant G/A snv 0.45 5
rs7523050
LOC107985159 ; AKNAD1 ; GPSM2
1.000 1 108875057 intron variant C/A snv 0.18 5
rs921231
SLC26A7
1.000 8 91348168 intron variant T/C snv 0.21 5
rs62621197
ADAMTS10
1.000 0.080 19 8605262 missense variant C/A;T snv 4.1E-06; 3.1E-02 2.9E-02 4
rs545608
CRYZL2P-SEC16B ; SEC16B
0.925 0.040 1 177929986 intron variant G/C snv 0.20 4
rs3812049
SLC12A2 ; LINC01184
5 128083158 non coding transcript exon variant C/A;G;T snv 4
rs2145270 20 6641038 regulatory region variant C/T snv 0.61 3
rs41310284 10 100687890 intergenic variant C/A;T snv 3
rs3817428
ACAN
15 88872016 missense variant C/G snv 0.20 0.20 3
rs4800148
CABLES1
18 23144364 intron variant G/A;C snv 3
rs41271299
ID4
6 19839184 intron variant C/A;G;T snv 3
rs314263
LIN28B
6 104944870 intron variant C/T snv 0.69 3
rs4694504 4 72630974 intergenic variant A/G;T snv 2
rs6492538 13 91341492 intergenic variant A/C snv 0.83 2
rs7306275 12 49856328 upstream gene variant G/A snv 0.29 2
rs994014 4 81244636 intergenic variant T/C snv 0.43 2