Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800888
ADRB2
0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 17
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 12
rs35107139
BMP4
0.776 0.080 14 53952388 intron variant A/C;G;T snv 11
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 10
rs2869966
LOC105377327 ; FAM13A
1.000 0.040 4 88947927 intron variant C/T snv 0.47 9
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 8
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs1799807
BCHE
0.925 0.240 3 165830741 missense variant T/C snv 1.2E-02 1.2E-02 6
rs1529672
RARB
1.000 0.040 3 25479091 intron variant C/A;T snv 6
rs7753012
ADGRG6
6 142424746 intron variant T/G snv 0.50 5
rs2798641
ARMC2
6 108946847 intron variant C/T snv 0.15 5
rs11722225
INTS12 ; GSTCD
4 105845273 intron variant T/C snv 5.5E-02 5
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
rs1192415 0.925 0.040 1 91611540 TF binding site variant G/A snv 0.81 4
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
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