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SNCA c.306+758C>T
Variant ID: 4-90742639-G-A
NM_000345.3(
SNCA
):c.306+758C>T
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 cytosine-thymine (CT)-rich haplotype in intron 4 of SNCA confers risk for Lewy body pathology in Alzheimer's disease and affects SNCA expression.
Alzheimer'S & Dementia : The Journal Of The Alzheimer'S Association
Lutz, Michael W MW; Saul, Robert R; Linnertz, Colton C; Glenn, Omolara-Chinue OC; Roses, Allen D AD; Chiba-Falek, Ornit O
Publication Date: 2015-10
Variant appearance in text: rs17016251
PubMed Link:
26079410
Variant Present in the following documents:
Main text
View BVdb publication page