CNNM2 c.1621+42104G>C

Variant ID: 10-104721962-G-C

NM_017649.4(CNNM2):c.1621+42104G>C

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Multimodal CRISPR perturbations of GWAS loci associated with coronary artery disease in vascular endothelial cells.

Plos Genetics
Wünnemann, Florian F; Fotsing Tadjo, Thierry T; Beaudoin, Mélissa M; Lalonde, Simon S; Lo, Ken Sin KS; Kleinstiver, Benjamin P BP; Lettre, Guillaume G
Publication Date: 2023-03-16

Variant appearance in text: rs78260931
PubMed Link: 36928188
Variant Present in the following documents:
  • Main text
  • pgen.1010680.pdf
View BVdb publication page