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Variant ID: 1-55518622-T-C
NM_174936.3(
PCSK9
):c.799+158T>C
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
The flashfm approach for fine-mapping multiple quantitative traits.
Nature Communications
Hernández, N N; Soenksen, J J; Newcombe, P P; Sandhu, M M; Barroso, I I; Wallace, C C; Asimit, J L JL
Publication Date: 2021-10-22
Variant appearance in text: rs45613943
PubMed Link:
34686674
Variant Present in the following documents:
Main text
41467_2021_Article_26364.pdf
View BVdb publication page
Cross-species regulatory sequence activity prediction.
Plos Computational Biology
Kelley, David R DR
Publication Date: 2020-07
Variant appearance in text: rs45613943
PubMed Link:
32687525
Variant Present in the following documents:
Main text
View BVdb publication page
Genetic associations between serum low LDL-cholesterol levels and variants in LDLR, APOB, PCSK9 and LDLRAP1 in African populations.
Plos One
Hayat, Mahtaab M; Kerr, Robyn R; Bentley, Amy R AR; Rotimi, Charles N CN; Raal, Frederick J FJ; Ramsay, Michèle M
Publication Date: 2020
Variant appearance in text: rs45613943
PubMed Link:
32084179
Variant Present in the following documents:
Main text
View BVdb publication page