Variant ID: 1-55513521-C-A

NM_174936.3(PCSK9):c.523+1202C>A

This variant was identified in 3 publications




Publications:


Variations of the proprotein convertase subtilisin/kexin type 9 gene in coronary artery disease.

The Journal Of International Medical Research
SM Chiang, YS Yang, SF Yang, CF Tsai, KC Ueng
Publication Date: 2019-04-05

Variant appearance in text: rs529787
PMID: 30947598
View BVdb publication page



Correlation of PCSK9 gene polymorphism with cerebral ischemic stroke in Xinjiang Han and Uygur populations.

Medical Science Monitor : International Medical Journal Of Experimental And Clinical Research
D Han, J Ma, X Zhang, J Cai, J Li, T Tuerxun, C Hao, L Du, J Lei
Publication Date: 2014-09-30

Variant appearance in text: N/A
PMID: 25266949
View BVdb publication page



PCSK9 SNP rs11591147 is associated with low cholesterol levels but not with cognitive performance or noncardiovascular clinical events in an elderly population.

Journal Of Lipid Research
I Postmus, S Trompet, AJ de Craen, BM Buckley, I Ford, DJ Stott, N Sattar, PE Slagboom, RG Westendorp, JW Jukema
Publication Date: 2013-02

Variant appearance in text: rs529787
PMID: 23300213
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.523+1202C>A - intron_variant - 3/11
ENST00000452118.2 c.523+1202C>A - intron_variant - 3/5
ENST00000543384.1 c.-77-4430C>A - intron_variant - 1/9
NM_174936.4 c.523+1202C>A - intron_variant - 3/11
NR_110451.1 n.183-4430C>A - intron_variant,non_coding_transcript_variant - 1/9