LRP1B c.6356C>G ;(p.T2119R)

Variant ID: 2-141459361-G-C

NM_018557.2(LRP1B):c.6356C>G;(p.T2119R)

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:

Rare Recurrent Variants in Noncoding Regions Impact Attention-Deficit Hyperactivity Disorder (ADHD) Gene Networks in Children of both African American and European American Ancestry.

Genes
Liu, Yichuan Y; Chang, Xiao X; Qu, Hui-Qi HQ; Tian, Lifeng L; Glessner, Joseph J; Qu, Jingchun J; Li, Dong D; Qiu, Haijun H; Sleiman, Patrick P; Hakonarson, Hakon H
Publication Date: 2021-02-22

Variant appearance in text: rs147598746
PubMed Link: 33671795
Variant Present in the following documents:
  • Main text
  • genes-12-00310.pdf
View BVdb publication page