Variant ID: 1-55522141-A-C

NM_174936.3(PCSK9):c.996+279A>C

This variant was identified in 1 publication



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

Publications:

Mendelian randomization: a novel approach for the prediction of adverse drug events and drug repurposing opportunities.

International Journal Of Epidemiology
VM Walker, G Davey Smith, NM Davies, RM Martin
Publication Date: 2017-12-01

Variant appearance in text: rs479910
PMID: 29040597
View BVdb publication page


Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.996+279A>C - intron_variant - 6/11
ENST00000490692.1 n.1817+279A>C - intron_variant,non_coding_transcript_variant - 3/7
ENST00000543384.1 c.396+279A>C - intron_variant - 4/9
NM_174936.4 c.996+279A>C - intron_variant - 6/11
NR_110451.1 n.655+279A>C - intron_variant,non_coding_transcript_variant - 4/9