Bibliome.ai browser hg19
Search
About
Stats
FAQ
NOX3 c.487-914C>A
Variant ID: 6-155762185-G-T
NM_015718.2(
NOX3
):c.487-914C>A
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:
Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
Genomics Insights
Driss, A A; Asare, K O KO; Hibbert, J M JM; Gee, B E BE; Adamkiewicz, T V TV; Stiles, J K JK
Publication Date: 2009-07-30
Variant appearance in text: rs6557420
PubMed Link:
20401335
Variant Present in the following documents:
Main text
gei-2-2009-023.pdf
View BVdb publication page