LRP1B c.5360-11948A>G

Variant ID: 2-141545755-T-C

NM_018557.2(LRP1B):c.5360-11948A>G

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 associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.

Human Molecular Genetics
Hromatka, Bethann S BS; Tung, Joyce Y JY; Kiefer, Amy K AK; Do, Chuong B CB; Hinds, David A DA; Eriksson, Nicholas N
Publication Date: 2015-05-01

Variant appearance in text: rs17515225
PubMed Link: 25628336
Variant Present in the following documents:
  • Main text
  • ddv028.pdf
View BVdb publication page