MSH2 c.1277-2383G>C

Variant ID: 2-47670304-G-C

NM_000251.2(MSH2):c.1277-2383G>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Inversion of exons 1-7 of the MSH2 gene is a frequent cause of unexplained Lynch syndrome in one local population.

Familial Cancer
Rhees, Jennifer J; Arnold, Mildred M; Boland, C Richard CR
Publication Date: 2014-06

Variant appearance in text: rs6726691
PubMed Link: 24114314
Variant Present in the following documents:
  • Main text
View BVdb publication page



Endometrial cancer and genetic variation in PTEN, PIK3CA, AKT1, MLH1, and MSH2 within a population-based case-control study.

Gynecologic Oncology
Lacey, James V JV; Yang, Hannah H; Gaudet, Mia M MM; Dunning, Alison A; Lissowska, Jolanta J; Sherman, Mark E ME; Peplonska, Beata B; Brinton, Louise A LA; Healey, Catherine S CS; Ahmed, Shahana S; Pharoah, Paul P; Easton, Douglas D; Chanock, Stephen S; Garcia-Closas, Montserrat M
Publication Date: 2011-02

Variant appearance in text: rs6726691
PubMed Link: 21093899
Variant Present in the following documents:
  • Main text
View BVdb publication page