Variant ID: 1-55525868-C-T

NM_174936.3(PCSK9):c.1681+532C>T

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: rs603247
PubMed Link: 31714636
Variant Present in the following documents:
  • ANA-87-30-s001.docx
View BVdb publication page



Genetic markers of lipid metabolism genes associated with low susceptibility to HCV infection.

Scientific Reports
LM Real, J Macías, A Rivero-Juárez, F Téllez, D Merino, S Moreno-Grau, A Orellana, J Gómez-Salgado, ME Sáez, M Frías, A Corma-Gómez, N Merchante, A Ruiz, A Caruz, JA Pineda,
Publication Date: 2019-06-21

Variant appearance in text: rs603247
PubMed Link: 31227787
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.1681+532C>T - intron_variant - 10/11
ENST00000490692.1 n.2228-1180C>T - intron_variant,non_coding_transcript_variant - 6/7
ENST00000543384.1 c.*228+532C>T - intron_variant - 8/9
NM_174936.4 c.1681+532C>T - intron_variant - 10/11
NR_110451.1 n.1288+532C>T - intron_variant,non_coding_transcript_variant - 8/9