Variant ID: 1-55526296-A-C

NM_174936.3(PCSK9):c.1682-752A>C

This variant was identified in 4 publications




Publications:


Association and differences in genetic polymorphisms in PCSK9 gene in subjects with lacunar infarction in the Han and Uygur populations of Xinjiang Uygur Autonomous Region of China.

Neural Regeneration Research
DF Han, JH Ma, CG Hao, Tuerhong Tuerxun, L Du, XN Zhang
Publication Date: 2017-08

Variant appearance in text: N/A
PMID: 28966647
View BVdb publication page



Association between the DOCK7, PCSK9 and GALNT2 Gene Polymorphisms and Serum Lipid levels.

Scientific Reports
T Guo, RX Yin, F Huang, LM Yao, WX Lin, SL Pan
Publication Date: 2016-01-08

Variant appearance in text: N/A
PMID: 26744084
View BVdb publication page



Association of the variants and haplotypes in the DOCK7, PCSK9 and GALNT2 genes and the risk of hyperlipidaemia.

Journal Of Cellular And Molecular Medicine
T Guo, RX Yin, WX Lin, W Wang, F Huang, SL Pan
Publication Date: 2016-02

Variant appearance in text: N/A
PMID: 26493351
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: rs615563
PMID: 23300213
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.1682-752A>C - intron_variant - 10/11
ENST00000490692.1 n.2228-752A>C - intron_variant,non_coding_transcript_variant - 6/7
ENST00000543384.1 c.*229-752A>C - intron_variant - 8/9
NM_174936.4 c.1682-752A>C - intron_variant - 10/11
NR_110451.1 n.1289-752A>C - intron_variant,non_coding_transcript_variant - 8/9