BMPR1B c.-17-14650T>C

Variant ID: 4-96010909-T-C

NM_001203.2(BMPR1B):c.-17-14650T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic variants and cell-free hemoglobin processing in sickle cell nephropathy.

Haematologica
Saraf, Santosh L SL; Zhang, Xu X; Shah, Binal B; Kanias, Tamir T; Gudehithlu, Krishnamurthy P KP; Kittles, Rick R; Machado, Roberto F RF; Arruda, Jose A L JA; Gladwin, Mark T MT; Singh, Ashok K AK; Gordeuk, Victor R VR
Publication Date: 2015-10

Variant appearance in text: rs1434549
PubMed Link: 26206798
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: rs1434549
PubMed Link: 20401335
Variant Present in the following documents:
  • Main text
  • gei-2-2009-023.pdf
View BVdb publication page