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.




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