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ABCG8 c.965-2345T>C
Variant ID: 2-44096770-T-C
NM_022437.2(
ABCG8
):c.965-2345T>C
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Genes Potentially Associated with Familial Hypercholesterolemia.
Biomolecules
Mikhailova, Svetlana S; Ivanoshchuk, Dinara D; Timoshchenko, Olga O; Shakhtshneider, Elena E
Publication Date: 2019-11-29
Variant appearance in text: rs4952688
PubMed Link:
31795497
Variant Present in the following documents:
Main text
biomolecules-09-00807.pdf
View BVdb publication page
Coherent somatic mutation in autoimmune disease.
Plos One
Ross, Kenneth Andrew KA
Publication Date: 2014
Variant appearance in text: rs4952688
PubMed Link:
24988487
Variant Present in the following documents:
Main text
pone.0101093.pdf
View BVdb publication page