Variant ID: 1-55522558-G-T

NM_174936.3(PCSK9):c.997-446G>T

This variant was identified in 1 publication



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

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: rs7525503
PubMed Link: 31714636
Variant Present in the following documents:
  • ANA-87-30-s001.docx
View BVdb publication page


Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.997-446G>T - intron_variant - 6/11
ENST00000490692.1 n.1818-543G>T - intron_variant,non_coding_transcript_variant - 3/7
ENST00000543384.1 c.397-446G>T - intron_variant - 4/9
NM_174936.4 c.997-446G>T - intron_variant - 6/11
NR_110451.1 n.656-446G>T - intron_variant,non_coding_transcript_variant - 4/9