OPN1LW c.511G>C ;(p.V171L)

Variant ID: X-153418514-G-C

NM_020061.4(OPN1LW):c.511G>C;(p.V171L)

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:

Insight from OPN1LW Gene Haplotypes into the Cause and Prevention of Myopia.

Genes
Neitz, Maureen M; Wagner-Schuman, Melissa M; Rowlan, Jessica S JS; Kuchenbecker, James A JA; Neitz, Jay J
Publication Date: 2022-05-25

Variant appearance in text: rs5986963
PubMed Link: 35741704
Variant Present in the following documents:
  • Main text
  • genes-13-00942.pdf
View BVdb publication page