Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2233679
PIN1 ; LOC100996288
0.763 0.360 19 9834678 splice region variant C/T snv 0.59 11
rs2494938
LRFN2
0.752 0.240 6 40568389 intron variant G/A snv 0.51 11
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 11
rs1048638
CA9
0.807 0.160 9 35681125 3 prime UTR variant C/A;G snv 10
rs1057519824
MET
0.807 0.120 7 116783374 missense variant T/G snv 10
rs1057519911
MAPK1
0.776 0.160 22 21772875 missense variant C/T snv 10
rs6059655
RALY
0.790 0.080 20 34077942 intron variant A/G snv 0.95 10
rs1194611372
S100A11
0.763 0.320 1 152032679 missense variant A/C snv 9
rs121918502
FGFR2
0.790 0.160 10 121517351 missense variant G/C snv 9
rs1458974438
STK11
0.807 0.080 19 1206957 missense variant G/A snv 9
rs28929495
EGFR
0.807 0.120 7 55174014 missense variant G/A;C;T snv 9
rs397517108
EGFR ; EGFR-AS1
0.790 0.120 7 55181312 missense variant GC/TT mnv 9
rs12210050
LOC105374875
0.807 0.040 6 475489 non coding transcript exon variant C/T snv 0.11 8
rs1801321
RAD51 ; RAD51-AS1
0.790 0.160 15 40695367 5 prime UTR variant G/C;T snv 0.35 8
rs4645978
CASP9 ; DNAJC16
0.827 0.120 1 15525539 intron variant C/A;T snv 8
rs10810657 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 7
rs2285947
DNAH11
0.807 0.120 7 21544470 intron variant G/A snv 0.44 7
rs2498801
LOC102723342 ; AKT1
0.790 0.120 14 104769221 upstream gene variant T/C snv 0.41 7
rs344781
PLAUR
0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80 7
rs7335046 0.807 0.040 13 99389484 downstream gene variant G/C snv 0.80 7
rs987525
CCDC26
0.807 0.160 8 128933908 intron variant C/A snv 0.31 7
rs1057520018
STK11
0.807 0.080 19 1223124 missense variant T/C snv 6
rs12108497
PRIMPOL ; CASP3
0.851 0.080 4 184650403 intron variant C/G;T snv 6
rs1389500636
EGFR
0.827 0.080 7 55156796 missense variant G/A snv 6
rs35407
SLC45A2
0.807 0.080 5 33946466 3 prime UTR variant A/C;G snv 6