Variant ID: 1-55509213-G-C

NM_174936.3(PCSK9):c.208-303G>C

This variant was identified in 6 publications




Publications:


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
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Evaluation of the effect of genetic variation on the relationship between statins, cardiovascular disease and cancer.

International Journal Of Molecular Epidemiology And Genetics
P Desai, A Jay, C Bock, G Dyson, T Okwuosa, MS Simon
Publication Date: 2013-11-28

Variant appearance in text: N/A
PMID: 24319534
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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: N/A
PMID: 23300213
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Genetic variability within the cholesterol lowering pathway and the effectiveness of statins in reducing the risk of MI.

Atherosclerosis
BJ Peters, H Pett, OH Klungel, BH Stricker, BM Psaty, NL Glazer, KL Wiggins, JC Bis, A de Boer, AH Maitland-van der Zee
Publication Date: 2011-08

Variant appearance in text: rs10888896
PMID: 21741043
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Complexity in the genetic architecture of leukoaraiosis in hypertensive sibships from the GENOA Study.

Bmc Medical Genomics
JA Smith, ST Turner, YV Sun, M Fornage, RJ Kelly, TH Mosley, CR Jack, IJ Kullo, SL Kardia
Publication Date: 2009-04-07

Variant appearance in text: N/A
PMID: 19351393
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Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.208-303G>C - intron_variant - 1/11
ENST00000452118.2 c.208-303G>C - intron_variant - 1/5
ENST00000543384.1 c.-78+3137G>C - intron_variant - 1/9
NM_174936.4 c.208-303G>C - intron_variant - 1/11
NR_110451.1 n.182+3137G>C - intron_variant,non_coding_transcript_variant - 1/9