Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs4409766
BORCS7-ASMT ; BORCS7
1.000 0.040 10 102856906 intron variant T/C snv 0.14 6
rs223331
CISD2
0.851 0.160 4 102872408 intron variant T/A;C snv 5
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs34911341
GHRL ; GHRLOS
0.882 0.200 3 10289835 missense variant C/T snv 7.0E-03 7.3E-03 5
rs26802
GHRLOS ; GHRL
0.925 0.160 3 10290681 intron variant T/G snv 0.31 3
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs11191514
CNNM2
10 103013607 intron variant C/G;T snv 2
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 10
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs12219304
NT5C2
10 103171827 intron variant G/C;T snv 1
rs11191593
NT5C2
10 103179458 intron variant T/C snv 9.0E-02 4
rs112913898 10 103199143 intergenic variant G/A snv 9.1E-02 3
rs8702
KLC1
0.851 0.160 14 103686015 3 prime UTR variant C/G snv 0.61 5
rs4387287
STN1
10 103918139 5 prime UTR variant A/C snv 0.69 4
rs117564807
COL17A1
10 104040357 missense variant C/G;T snv 1.9E-03 1
rs7950273
PDGFD
0.925 0.120 11 104160870 intron variant C/G snv 0.32 5
rs28868104 1.000 0.080 3 104241993 intergenic variant C/T snv 0.17 2
rs530391015
INF2
0.882 0.080 14 104703445 stop gained G/A;C;T snv 4.0E-06 5
rs2066715
ABCA1
0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02 7
rs138533962
STYK1
12 10620278 missense variant G/A;T snv 4.0E-05; 8.0E-06 1
rs2569512
ILF3
0.925 0.080 19 10679486 intron variant T/C snv 0.76 5
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs12046278
CASZ1
1 10739520 intron variant T/C snv 0.36 3