CHRNB2 c.101A>G ;(p.E34G)

Variant ID: 1-154541974-A-G

NM_000748.2(CHRNB2):c.101A>G;(p.E34G)

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:

The contribution of rare and common variants in 30 genes to risk nicotine dependence.

Molecular Psychiatry
Yang, J J; Wang, S S; Yang, Z Z; Hodgkinson, C A CA; Iarikova, P P; Ma, J Z JZ; Payne, T J TJ; Goldman, D D; Li, M D MD
Publication Date: 2015-11

Variant appearance in text: CHRNB2: E34G; rs200223952
PubMed Link: 25450229
Variant Present in the following documents:
  • Main text
  • nihms634433.pdf
View BVdb publication page