DisGeNET - a database of gene-disease associations

Hereditary Nonpolyposis Colorectal Neoplasms, C0009405

Variant: rs587781626 ×

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs587781626

PMS2

0.700

CausalMutation

CLINVAR

PMS2 monoallelic mutation carriers: the known unknown.

25856668

2016

dbSNP:

rs587781626

PMS2

0.700

CausalMutation

CLINVAR

The frequency of previously undetectable deletions involving 3' Exons of the PMS2 gene.

23012243

2013

dbSNP:

rs587781626

PMS2

0.700

CausalMutation

CLINVAR

Identification of Lynch syndrome mutations in the MLH1-PMS2 interface that disturb dimerization and mismatch repair.

20533529

2010

dbSNP:

rs587781626

PMS2

0.700

CausalMutation

CLINVAR

Truncation of the C-terminus of human MLH1 blocks intracellular stabilization of PMS2 and disrupts DNA mismatch repair.

16338176

2006

dbSNP:

rs587781626

PMS2

0.700

CausalMutation

CLINVAR

The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer.

10037723

1999