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TNNT2 c.68-8A>G
Variant ID: 1-201338981-T-C
NM_001276345.1(
TNNT2
):c.68-8A>G
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Clinical features, spectrum of causal genetic mutations and outcome of hypertrophic cardiomyopathy in South Africans.
Cardiovascular Journal Of Africa
Ntusi, Ntobeko A NA; Shaboodien, Gasnat G; Badri, Motasim M; Gumedze, Freedom F; Mayosi, Bongani M BM
Publication Date: 2016
Variant appearance in text: rs115805892
PubMed Link:
27841901
Variant Present in the following documents:
Main text
cvja-27-152.pdf
View BVdb publication page