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.




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