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PLCG1 c.217+3477T>A
Variant ID: 20-39769975-T-A
NM_002660.2(
PLCG1
):c.217+3477T>A
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
A systems biology approach uncovers cell-specific gene regulatory effects of genetic associations in multiple sclerosis.
Nature Communications
,
Publication Date: 2019-05-20
Variant appearance in text: rs3795131
PubMed Link:
31110181
Variant Present in the following documents:
41467_2019_9773_MOESM37_ESM.xlsx, sheet 1
41467_2019_9773_MOESM36_ESM.xlsx, sheet 1
View BVdb publication page
Low LDL cholesterol, PCSK9 and HMGCR genetic variation, and risk of Alzheimer's disease and Parkinson's disease: Mendelian randomisation study.
Bmj (Clinical Research Ed.)
Benn, Marianne M; Nordestgaard, Børge G BG; Frikke-Schmidt, Ruth R; Tybjærg-Hansen, Anne A
Publication Date: 2017-04-24
Variant appearance in text: rs3795131
PubMed Link:
28438747
Variant Present in the following documents:
benm033277.ww1.pdf
View BVdb publication page