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LRP1B c.2887+9830G>T
Variant ID: 2-141729899-C-A
NM_018557.2(
LRP1B
):c.2887+9830G>T
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 Variants behind Cardiovascular Diseases and Dementia.
Genes
Ho, Wei-Min WM; Wu, Yah-Yuan YY; Chen, Yi-Chun YC
Publication Date: 2020-12-18
Variant appearance in text: rs10201482
PubMed Link:
33352859
Variant Present in the following documents:
Main text
genes-11-01514.pdf
View BVdb publication page