Variant ID: 1-55525726-T-G

NM_174936.3(PCSK9):c.1681+390T>G

This variant was identified in 2 publications




Publications:


Lipid lowering and Alzheimer disease risk: A mendelian randomization study.

Annals Of Neurology
DM Williams, C Finan, AF Schmidt, S Burgess, AD Hingorani
Publication Date: 2020-01

Variant appearance in text: rs602705
PubMed Link: 31714636
Variant Present in the following documents:
  • ANA-87-30-s001.docx
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.)
M Benn, BG Nordestgaard, R Frikke-Schmidt, A Tybjærg-Hansen
Publication Date: 2017-04-24

Variant appearance in text: rs602705
PubMed Link: 28438747
Variant Present in the following documents:
  • benm033277.ww1.pdf
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.1681+390T>G - intron_variant - 10/11
ENST00000490692.1 n.2228-1322T>G - intron_variant,non_coding_transcript_variant - 6/7
ENST00000543384.1 c.*228+390T>G - intron_variant - 8/9
NM_174936.4 c.1681+390T>G - intron_variant - 10/11
NR_110451.1 n.1288+390T>G - intron_variant,non_coding_transcript_variant - 8/9