SELP c.1147+220G>A

Variant ID: 1-169580510-C-T

NM_003005.3(SELP):c.1147+220G>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


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: rs3917733
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: rs3917733
PubMed Link: 20401335
Variant Present in the following documents:
  • Main text
  • gei-2-2009-023.pdf
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: rs3917733
PubMed Link: 15778708
Variant Present in the following documents:
  • Main text
View BVdb publication page