SNCA c.306+35494G>A

Variant ID: 4-90707903-C-T

NM_000345.3(SNCA):c.306+35494G>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:

A systematic review of associations between common SNCA variants and clinical heterogeneity in Parkinson's disease.

Npj Parkinson'S Disease
Pedersen, Camilla Christina CC; Lange, Johannes J; Førland, Marthe Gurine Gunnarsdatter MGG; Macleod, Angus D AD; Alves, Guido G; Maple-Grødem, Jodi J
Publication Date: 2021-07-01

Variant appearance in text: rs3775438
PubMed Link: 34210990
Variant Present in the following documents:
  • 41531_2021_196_MOESM1_ESM.pdf
View BVdb publication page