NF2 c.1738-2299T>C

Variant ID: 22-30088442-T-C

NM_000268.3(NF2):c.1738-2299T>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:

A new model calling procedure for Illumina BeadArray data.

Bmc Genetics
Li, Gengxin G
Publication Date: 2016-06-24

Variant appearance in text: rs1009148
PubMed Link: 27343118
Variant Present in the following documents:
  • Main text
  • 12863_2016_Article_398.pdf
View BVdb publication page