Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs10906850
LOC105376434
1.000 0.080 10 15183055 regulatory region variant T/C snv 0.29 2
rs10951982
RAC1
0.851 0.160 7 6382925 intron variant G/A;T snv 5
rs11011653
PLXDC2
1.000 0.080 10 19875064 intron variant A/G;T snv 2
rs11089781
APOL3
0.925 0.080 22 36160720 stop gained G/A snv 1.6E-02 6.5E-02 2
rs11089788
MYH9
0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs11123169
PSD4
1.000 0.080 2 113209498 upstream gene variant C/A;T snv 3
rs11128347
PDZRN3
1.000 0.080 3 73570410 intron variant G/C;T snv 0.13 1
rs112201728
SLC22A1
1.000 0.080 6 160130454 intron variant C/A;T snv 2
rs112329286
SYNE2
1.000 0.080 14 63773159 intron variant -/ATTT delins 0.24 4
rs112407915 1.000 0.080 3 5505762 intergenic variant T/A snv 1.6E-02 1
rs11320420
MYRF ; TMEM258
1.000 0.080 11 61774535 intron variant AAAAA/-;AAA;AAAA;AAAAAA delins 0.30 2
rs114425659 1.000 0.080 4 117920116 intergenic variant G/A snv 4.9E-02 1
rs1145077
GATM
1.000 0.080 15 45391597 intron variant G/T snv 0.56 2
rs115007604
LINC02284
1.000 0.080 14 56358353 intron variant G/A snv 6.5E-03 1
rs115489112
NPHS1
0.925 0.080 19 35830918 missense variant G/A snv 4.3E-04 1.6E-03 2
rs11571317
CTLA4
0.882 0.160 2 203867285 upstream gene variant C/T snv 5.2E-02 3
rs115747230 1.000 0.080 9 76994030 downstream gene variant T/C snv 1.8E-02 1
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11622435
LOC101928462
0.827 0.120 14 81151652 intron variant G/A snv 4.7E-02 7
rs1162592300
ALB
0.925 0.080 4 73412045 missense variant G/A snv 3
rs11643718
SLC12A3
0.807 0.240 16 56899607 missense variant G/A snv 0.11 8.4E-02 10
rs11645800 1.000 0.080 16 62966386 intergenic variant A/G snv 0.19 1
rs116510623 1.000 0.080 11 24209937 intergenic variant A/G snv 2.6E-02 1
rs11662622 1.000 0.080 18 65592400 intergenic variant A/G snv 0.20 2