Variant ID: 1-55525944-G-A

NM_174936.3(PCSK9):c.1681+608G>A

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: rs114162366
PubMed Link: 31714636
Variant Present in the following documents:
  • ANA-87-30-s001.docx
View BVdb publication page



Genetic loci associated with coronary artery disease harbor evidence of selection and antagonistic pleiotropy.

Plos Genetics
SG Byars, QQ Huang, LA Gray, A Bakshi, S Ripatti, G Abraham, SC Stearns, M Inouye
Publication Date: 2017-06

Variant appearance in text: rs114162366
PubMed Link: 28640878
Variant Present in the following documents:
  • pgen.1006328.s005.pdf
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.1681+608G>A - intron_variant - 10/11
ENST00000490692.1 n.2228-1104G>A - intron_variant,non_coding_transcript_variant - 6/7
ENST00000543384.1 c.*228+608G>A - intron_variant - 8/9
NM_174936.4 c.1681+608G>A - intron_variant - 10/11
NR_110451.1 n.1288+608G>A - intron_variant,non_coding_transcript_variant - 8/9