APOE c.145G>C ;(p.G49R)

Variant ID: 19-45411118-G-C

NM_000041.2(APOE):c.145G>C;(p.G49R)

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:

Genetic Programming of Hypertension.

Frontiers In Pediatrics
Ahn, Sun-Young SY; Gupta, Charu C
Publication Date: 2017

Variant appearance in text: APOE: Gly49Arg
PubMed Link: 29404309
Variant Present in the following documents:
  • Main text
View BVdb publication page