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APOB c.35T>C ;(p.L12P)
Variant ID: 2-21266783-A-G
NM_000384.2(
APOB
):c.35T>C;(p.L12P)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Rare and common variants of APOB and PCSK9 in Korean patients with extremely low low-density lipoprotein-cholesterol levels.
Plos One
Lee, Chan Joo CJ; Lee, Yunbeom Y; Park, Sungha S; Kang, Seok-Min SM; Jang, Yangsoo Y; Lee, Ji Hyun JH; Lee, Sang-Hak SH
Publication Date: 2017
Variant appearance in text: APOB: L12P; rs758450840
PubMed Link:
29036232
Variant Present in the following documents:
Main text
pone.0186446.pdf
View BVdb publication page