Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913483
FGFR3
0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 31
rs17577
SLC12A5-AS1 ; MMP9
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs1805007
MC1R
0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 25
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs1801270
CDKN1A
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05 22
rs1800975
XPA
0.701 0.360 9 97697296 5 prime UTR variant T/C;G snv 0.63; 4.5E-06; 4.5E-06 19
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 15
rs2233678
PIN1 ; LOC100996288
0.732 0.360 19 9834503 non coding transcript exon variant G/A;C snv 14
rs16891982
SLC45A2
0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 13
rs3813867
LOC107984284 ; CYP2E1
0.732 0.240 10 133526101 intron variant G/A;C snv 13
rs749140677
VDR
0.752 0.240 12 47857185 missense variant G/A snv 8.0E-06 13
rs1057520004
TP53
0.752 0.240 17 7674884 missense variant A/C;T snv 12
rs121913465
EGFR ; EGFR-AS1
0.763 0.160 7 55181312 missense variant G/T snv 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
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