Variant ID: 1-55527323-G-A

NM_174936.3(PCSK9):c.1863+94G>A

This variant was identified in 2 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: rs630431
PMID: 28966647
View BVdb publication page



Exploring the interaction between SNP genotype and postmenopausal hormone therapy effects on stroke risk.

Genome Medicine
Y Huang, DG Ballinger, R Stokowski, E Beilharz, JG Robinson, S Liu, RD Robinson, VW Henderson, JE Rossouw, RL Prentice
Publication Date: 2012

Variant appearance in text: rs630431
PMID: 22794791
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.1863+94G>A - intron_variant - 11/11
ENST00000490692.1 n.2409+94G>A - intron_variant,non_coding_transcript_variant - 7/7
ENST00000543384.1 c.*410+94G>A - intron_variant - 9/9
NM_174936.4 c.1863+94G>A - intron_variant - 11/11
NR_110451.1 n.1470+94G>A - intron_variant,non_coding_transcript_variant - 9/9