MSH2 c.1277-2297G>A

Variant ID: 2-47670390-G-A

NM_000251.2(MSH2):c.1277-2297G>A

This variant was identified in 1 publication

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: rs6726832
PubMed Link: 24114314
Variant Present in the following documents:
  • Main text
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