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CP c.1864+62T>C
Variant ID: 3-148905777-A-G
NM_000096.3(
CP
):c.1864+62T>C
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:
Analysis of nucleotide variations in genes of iron management in patients of Parkinson's disease and other movement disorders.
Parkinson'S Disease
Castiglioni, Emanuela E; Finazzi, Dario D; Goldwurm, Stefano S; Pezzoli, Gianni G; Forni, Gianluca G; Girelli, Domenico D; Maccarinelli, Federica F; Poli, Maura M; Ferrari, Maurizio M; Cremonesi, Laura L; Arosio, Paolo P
Publication Date: 2010-10-17
Variant appearance in text: rs35149808
PubMed Link:
20981230
Variant Present in the following documents:
Main text
PD2011-827693.pdf
View BVdb publication page