MSH2 c.1386+7377G>T

Variant ID: 2-47680173-G-T

NM_000251.2(MSH2):c.1386+7377G>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Unique DNA repair gene variations and potential associations with the primary antibody deficiency syndromes IgAD and CVID.

Plos One
Offer, Steven M SM; Pan-Hammarström, Qiang Q; Hammarström, Lennart L; Harris, Reuben S RS
Publication Date: 2010-08-18

Variant appearance in text: rs3771276
PubMed Link: 20805886
Variant Present in the following documents:
  • Main text
  • pone.0012260.pdf
View BVdb publication page