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
rs35107139
BMP4
0.776 0.080 14 53952388 intron variant A/C;G;T snv 11
rs2145272 20 6645571 intergenic variant G/A;T snv 7
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 6
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 6
rs2869966
LOC105377327 ; FAM13A
1.000 0.040 4 88947927 intron variant C/T snv 0.47 6
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 6
rs34712979
NPNT
1.000 0.040 4 105897896 splice region variant G/A;T snv 0.17 5
rs755249
PPIEL ; BMP8A
1 39529402 3 prime UTR variant C/A;T snv 5
rs6780171
IGF2BP2
3 185785668 intron variant T/A snv 0.39 4
rs1513272
JAZF1
7 28160478 intron variant C/T snv 0.40 4
rs13116999
LOC105377462
4 144521212 intron variant G/A snv 0.65 4
rs1529672
RARB
1.000 0.040 3 25479091 intron variant C/A;T snv 4
rs7424771
RBMS1
2 160419867 intron variant G/A snv 0.44 4
rs7752448
ZSCAN31
6 28333322 intron variant A/G snv 0.15 4
rs1102077 6 139950220 intron variant A/C snv 0.21 3
rs11176001 12 66015587 regulatory region variant C/A snv 9.6E-02 3
rs1192415 0.925 0.040 1 91611540 TF binding site variant G/A snv 0.81 3
rs12331869 4 55145982 intergenic variant A/G snv 0.76 3
rs12481092 20 46858178 upstream gene variant C/T snv 0.21 3
rs12698403 7 156334552 intergenic variant G/A snv 0.40 3
rs12707691 7 84940194 non coding transcript exon variant C/G snv 0.24 3
rs12811814 12 4134583 intergenic variant T/C snv 0.45 3
rs12945803 17 48474867 upstream gene variant T/C snv 0.19 3