Source: UNIPROT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 5
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs80358451
BRCA2
0.925 0.160 13 32333140 missense variant T/G snv 5.6E-05 6.3E-05 2
rs104894094
CDKN2A
0.763 0.200 9 21971058 missense variant C/A;G;T snv 8.5E-06; 4.3E-06 2
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 2
rs17107315
SPINK1
0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 2
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs121913527
KRAS
0.807 0.320 12 25225628 missense variant C/A;G;T snv 1
rs11554495
KRT8
0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 1
rs149617956
MITF
0.672 0.560 3 69964940 missense variant G/A snv 1.4E-03 1.6E-03 1
rs587779067
MSH2
0.882 0.200 2 47416399 missense variant C/G;T snv 1
rs34612342
MUTYH
0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 1
rs267606982
PRSS1
0.742 0.120 7 142751938 missense variant GC/AT mnv 1
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 1
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 1
rs1555525012
TP53
0.882 0.200 17 7673603 missense variant G/A snv 1
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 1