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MYH7 c.4353+42G>A
Variant ID: 14-23886670-C-T
NM_000257.2(
MYH7
):c.4353+42G>A
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:
Association of long-chain non-coding RNA MHRT gene single nucleotide polymorphism with risk and prognosis of chronic heart failure.
Medicine
Zhang, Gao G; Dou, Liping L; Chen, Yuanyuan Y
Publication Date: 2020-07-17
Variant appearance in text: rs3729822
PubMed Link:
32702806
Variant Present in the following documents:
Main text
medi-99-e19703.pdf
View BVdb publication page
Sources of discordance among germ-line variant classifications in ClinVar.
Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Yang, Shan S; Lincoln, Stephen E SE; Kobayashi, Yuya Y; Nykamp, Keith K; Nussbaum, Robert L RL; Topper, Scott S
Publication Date: 2017-10
Variant appearance in text: MYH7: 4353+42G>A
PubMed Link:
28569743
Variant Present in the following documents:
gim201760x7.xlsx, sheet 2
View BVdb publication page