MET c.-14-1476G>A

Variant ID: 7-116337649-G-A

NM_000245.2(MET):c.-14-1476G>A

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Lymphatic and angiogenic candidate genes predict the development of secondary lymphedema following breast cancer surgery.

Plos One
Miaskowski, Christine C; Dodd, Marylin M; Paul, Steven M SM; West, Claudia C; Hamolsky, Deborah D; Abrams, Gary G; Cooper, Bruce A BA; Elboim, Charles C; Neuhaus, John J; Schmidt, Brian L BL; Smoot, Betty B; Aouizerat, Bradley E BE
Publication Date: 2013

Variant appearance in text: rs38850
PubMed Link: 23613720
Variant Present in the following documents:
  • Main text
  • pone.0060164.pdf
View BVdb publication page



Genetics of chronic rhinosinusitis: state of the field and directions forward.

The Journal Of Allergy And Clinical Immunology
Hsu, Joy J; Avila, Pedro C PC; Kern, Robert C RC; Hayes, M Geoffrey MG; Schleimer, Robert P RP; Pinto, Jayant M JM
Publication Date: 2013-04

Variant appearance in text: rs38850
PubMed Link: 23540616
Variant Present in the following documents:
  • Main text
View BVdb publication page



Polymorphisms in RYBP and AOAH genes are associated with chronic rhinosinusitis in a Chinese population: a replication study.

Plos One
Zhang, Yuan Y; Endam, Leandra Mfuna LM; Filali-Mouhim, Abdelali A; Zhao, Liping L; Desrosiers, Martin M; Han, Demin D; Zhang, Luo L
Publication Date: 2012

Variant appearance in text: rs38850
PubMed Link: 22723975
Variant Present in the following documents:
  • Main text
  • pone.0039247.pdf
View BVdb publication page



Genetic predictors for stroke in children with sickle cell anemia.

Blood
Flanagan, Jonathan M JM; Frohlich, Denise M DM; Howard, Thad A TA; Schultz, William H WH; Driscoll, Catherine C; Nagasubramanian, Ramamoorthy R; Mortier, Nicole A NA; Kimble, Amy C AC; Aygun, Banu B; Adams, Robert J RJ; Helms, Ronald W RW; Ware, Russell E RE
Publication Date: 2011-06-16

Variant appearance in text: rs38850
PubMed Link: 21515823
Variant Present in the following documents:
  • Main text
View BVdb publication page



Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.

Genomics Insights
Driss, A A; Asare, K O KO; Hibbert, J M JM; Gee, B E BE; Adamkiewicz, T V TV; Stiles, J K JK
Publication Date: 2009-07-30

Variant appearance in text: rs38850
PubMed Link: 20401335
Variant Present in the following documents:
  • Main text
  • gei-2-2009-023.pdf
View BVdb publication page



MET and autism susceptibility: family and case-control studies.

European Journal Of Human Genetics : Ejhg
Sousa, InĂªs I; Clark, Taane G TG; Toma, Claudio C; Kobayashi, Kazuhiro K; Choma, Maja M; Holt, Richard R; Sykes, Nuala H NH; Lamb, Janine A JA; Bailey, Anthony J AJ; Battaglia, Agatino A; Maestrini, Elena E; Monaco, Anthony P AP; ,
Publication Date: 2009-06

Variant appearance in text: rs38850
PubMed Link: 19002214
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia.

Nature Genetics
Sebastiani, Paola P; Ramoni, Marco F MF; Nolan, Vikki V; Baldwin, Clinton T CT; Steinberg, Martin H MH
Publication Date: 2005-04

Variant appearance in text: rs38850
PubMed Link: 15778708
Variant Present in the following documents:
  • Main text
View BVdb publication page