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MYL2 c.3+604C>T
Variant ID: 12-111357727-G-A
NM_000432.3(
MYL2
):c.3+604C>T
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:
Circulating white blood cells and lung function impairment: the observational studies and Mendelian randomization analysis.
Annals Of Medicine
Wu, Xiulong X; Wang, Chenming C; Li, Hang H; Meng, Hua H; Jie, Jiali J; Fu, Ming M; Bai, Yansen Y; Li, Guyanan G; Wei, Wei W; Feng, Yue Y; Li, Mengying M; Guan, Xin X; He, Meian M; Zhang, Xiaomin X; Guo, Huan H
Publication Date: 2021-12
Variant appearance in text: rs2040571
PubMed Link:
34259107
Variant Present in the following documents:
IANN_A_1948603_SM3508.pdf
View BVdb publication page
Whole gene sequencing identifies deep-intronic variants with potential functional impact in patients with hypertrophic cardiomyopathy.
Plos One
Mendes de Almeida, Rita R; Tavares, Joana J; Martins, Sandra S; Carvalho, Teresa T; Enguita, Francisco J FJ; Brito, Dulce D; Carmo-Fonseca, Maria M; Lopes, Luís Rocha LR
Publication Date: 2017
Variant appearance in text: MYL2: 3+604C>T; rs2040571
PubMed Link:
28797094
Variant Present in the following documents:
Main text
pone.0182946.pdf
View BVdb publication page