Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4806942
GIPC3
1.000 0.120 19 3589341 intron variant G/A snv 0.13 1
rs4919862
BSG
1.000 0.120 19 582253 intron variant T/C snv 0.82 1
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs112735431
RNF213 ; RNF213-AS1
0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs1057335
SERPINF2
0.827 0.120 17 1754359 missense variant G/A snv 0.22 0.20 5
rs13412
P3H4 ; FKBP10
1.000 0.120 17 41811190 missense variant T/A;C snv 0.38 0.34 1
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs2249825
HMGB1
0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs10507391
ALOX5AP
0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs9551963
ALOX5AP
0.851 0.160 13 30758410 intron variant A/C;T snv 6
rs9579646
ALOX5AP
0.851 0.160 13 30736442 intron variant G/A;T snv 6
rs4073259
ALOX5AP
0.882 0.160 13 30732134 intron variant G/A snv 0.49 4
rs755703581
PDX1
0.925 0.120 13 27920295 missense variant G/A snv 2.3E-05 7.0E-06 3
rs4147064
ALOX5AP
1.000 0.120 13 30745981 intron variant T/C snv 0.50 2
rs4769055
ALOX5AP
1.000 0.120 13 30735693 intron variant C/A snv 0.41 0.47 1
rs494860
PCID2 ; PROZ
1.000 0.120 13 113164695 intron variant T/A snv 0.26 0.19 1
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs6218
LINC02456 ; HELLPAR ; IGF1
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
rs10846744
SCARB1
0.763 0.160 12 124827879 intron variant G/C snv 0.32 11
rs5888
SCARB1
0.752 0.200 12 124800202 synonymous variant A/G;T snv 0.59; 4.0E-06 11
rs11833579 0.827 0.200 12 666033 upstream gene variant G/A snv 0.25 6
rs2162679
IGF1
0.851 0.240 12 102477481 intron variant C/G;T snv 6
rs1050283
OLR1
0.882 0.160 12 10159690 3 prime UTR variant G/A snv 0.40 4