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TCN2 c.*683A>C
Variant ID: 22-31023191-A-C
NM_000355.3(
TCN2
):c.*683A>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:
MicroRNA-binding site polymorphisms and risk of colorectal cancer: A systematic review and meta-analysis.
Cancer Medicine
Gholami, Morteza M; Larijani, Bagher B; Sharifi, Farshad F; Hasani-Ranjbar, Shirin S; Taslimi, Reza R; Bastami, Milad M; Atlasi, Rasha R; Amoli, Mahsa M MM
Publication Date: 2019-12
Variant appearance in text: rs1544468
PubMed Link:
31637880
Variant Present in the following documents:
Main text
CAM4-8-7477.pdf
View BVdb publication page
GENE-LEVEL PHARMACOGENETIC ANALYSIS ON SURVIVAL OUTCOMES USING GENE-TRAIT SIMILARITY REGRESSION.
The Annals Of Applied Statistics
Tzeng, Jung-Ying JY; Lu, Wenbin W; Hsu, Fang-Chi FC
Publication Date: 2014
Variant appearance in text: rs1544468
PubMed Link:
25018788
Variant Present in the following documents:
Main text
View BVdb publication page
Transcobalamin 2 variant associated with poststroke homocysteine modifies recurrent stroke risk.
Neurology
Hsu, F-C FC; Sides, E G EG; Mychaleckyj, J C JC; Worrall, B B BB; Elias, G A GA; Liu, Y Y; Chen, W-M WM; Coull, B M BM; Toole, J F JF; Rich, S S SS; Furie, K L KL; Sale, M M MM
Publication Date: 2011-10-18
Variant appearance in text: rs1544468
PubMed Link:
21975197
Variant Present in the following documents:
Main text
View BVdb publication page