Variant ID: 1-55507285-T-C

NM_174936.3(PCSK9):c.207+1568T>C

This variant was identified in 1 publication




Publications:


Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array.

European Journal Of Human Genetics : Ejhg
S Rodriguez, TR Gaunt, Y Guo, J Zheng, MR Barnes, W Tang, F Danish, A Johnson, BA Castillo, YR Li, H Hakonarson, SG Buxbaum, T Palmer, MY Tsai, LA Lange, S Ebrahim, G Davey Smith, DA Lawlor, AR Folsom, R Hoogeveen, A Reiner, B Keating, IN Day
Publication Date: 2016-01

Variant appearance in text: rs28385705
PMID: 25920552
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.207+1568T>C - intron_variant - 1/11
ENST00000452118.2 c.207+1568T>C - intron_variant - 1/5
ENST00000543384.1 c.-78+1209T>C - intron_variant - 1/9
NM_174936.4 c.207+1568T>C - intron_variant - 1/11
NR_110451.1 n.182+1209T>C - intron_variant,non_coding_transcript_variant - 1/9