Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121434596
rs121434596
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.740 1.000 1 2014 2016
dbSNP: rs104893829
rs104893829
VHL
0.882 0.240 3 10142088 missense variant C/T snv 2.0E-04 3.8E-04
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.720 1.000 1 2013 2017
dbSNP: rs1057519836
rs1057519836
3 41224630 missense variant A/C;G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519837
rs1057519837
1.000 0.040 3 41224631 missense variant C/G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.710 1.000 1 2011 2014
dbSNP: rs121913279
rs121913279
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.800 0.909 1 2006 2019
dbSNP: rs5030828
rs5030828
VHL
3 10142101 missense variant T/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519757
rs1057519757
0.882 0.120 5 68293310 missense variant G/A;C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 2 2010 2014
dbSNP: rs773686816
rs773686816
5 68295271 missense variant C/A;G;T snv 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 2 2014 2014
dbSNP: rs1057519838
rs1057519838
0.882 0.160 5 68293790 stop gained C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519839
rs1057519839
5 68295257 missense variant G/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519840
rs1057519840
5 68295257 inframe deletion GACAAACGTATGAACAGC/- del
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519841
rs1057519841
0.925 0.120 5 68295269 missense variant A/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519842
rs1057519842
5 68295304 inframe deletion CGA/- delins
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519843
rs1057519843
APC
5 112839522 frameshift variant AAGATTGGAAC/- del
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519844
rs1057519844
APC
5 112839522 frameshift variant AAGATTGGAACTAGGTCAGC/- del
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519845
rs1057519845
APC
5 112839990 frameshift variant GGACC/- del
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519846
rs1057519846
APC
5 112840263 frameshift variant ATTGATTC/- del
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1131692242
rs1131692242
5 68293722 inframe deletion AGA/- delins
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1131692243
rs1131692243
5 68295419 splice region variant GGT/- delins
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs121913390
rs121913390
5 150073481 stop gained A/G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs121913392
rs121913392
5 150054081 stop gained A/C;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs121913393
rs121913393
5 150054083 missense variant A/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1801271
rs1801271
5 150054082 missense variant T/A;C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs121913355
rs121913355
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.730 0.800 2 2004 2015
dbSNP: rs1057519824
rs1057519824
MET
0.807 0.120 7 116783374 missense variant T/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.710 1.000 1 2003 2007