GRIN2A c.414+78271G>C

Variant ID: 16-10195584-C-G

NM_001134407.1(GRIN2A):c.414+78271G>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:

Modeling X Chromosome Data Using Random Forests: Conquering Sex Bias.

Genetic Epidemiology
Winham, Stacey J SJ; Jenkins, Gregory D GD; Biernacka, Joanna M JM
Publication Date: 2016-02

Variant appearance in text: rs7205180
PubMed Link: 26639183
Variant Present in the following documents:
  • Main text
View BVdb publication page