Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121909233
KLLN ; PTEN
1.000 0.040 10 87864524 missense variant G/A snv 1
rs121909234
PTEN
1.000 0.040 10 87957867 missense variant G/A snv 1
rs137853080
STK11
1.000 0.040 19 1207058 missense variant T/G snv 1
rs137853081
STK11
1.000 0.040 19 1219352 missense variant G/C;T snv 1
rs1554653960
CDKN2A
0.925 0.040 9 21971007 missense variant C/T snv 1
rs200476704
TRAPPC1 ; CNTROB ; KCNAB3
1.000 0.040 17 7930659 stop gained G/A;C snv 2.4E-05 1
rs36204594
CDKN2A
1.000 0.040 9 21971180 missense variant G/A;T snv 1
rs397514644
AKT1
0.925 0.040 14 104780190 missense variant G/A snv 7.0E-06 1
rs80359204
BRCA2
1.000 0.040 13 32394741 missense variant A/G snv 1
rs137854599
CDKN2A
0.882 0.080 9 21971093 missense variant C/G;T snv 1
rs758389471
CDKN2A
0.882 0.080 9 21971160 missense variant C/G;T snv 4.7E-06; 4.7E-06 1
rs104894095
CDKN2A
0.827 0.120 9 21971200 missense variant C/G;T snv 9.0E-06 1
rs1057519713
KIT
0.925 0.120 4 54736498 missense variant G/C snv 1
rs121913386
CDKN2A
0.807 0.120 9 21971018 missense variant G/A;T snv 1
rs121913517
KIT
0.851 0.120 4 54727444 missense variant T/A;C;G snv 1
rs137854567
APC
0.882 0.120 5 112819272 missense variant C/A;G;T snv 4.0E-06; 6.7E-04 1
rs587782228
MUTYH
0.882 0.120 1 45330557 missense variant C/A;T snv 4.2E-06; 4.2E-06 1
rs878853647
CDKN2A
0.882 0.120 9 21971099 missense variant C/G;T snv 1
rs121913315
STK11
0.882 0.160 19 1220488 missense variant G/A;T snv 2
rs104894094
CDKN2A
0.763 0.200 9 21971058 missense variant C/A;G;T snv 8.5E-06; 4.3E-06 2
rs1064794292
CDKN2A
0.882 0.200 9 21974760 missense variant C/T snv 2
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 2
rs28931588
CTNNB1
0.701 0.200 3 41224606 missense variant G/A;C;T snv 2
rs104894098
CDKN2A
0.851 0.200 9 21970982 missense variant A/T snv 1
rs104894099
CDKN2A
0.851 0.200 9 21971183 missense variant A/C;T snv 4.6E-06 1