MAP3K7 c.1640+485G>A

Variant ID: 6-91227681-C-T

NM_145331.2(MAP3K7):c.1640+485G>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


The search for genetic modifiers of disease severity in the β-hemoglobinopathies.

Cold Spring Harbor Perspectives In Medicine
Lettre, Guillaume G
Publication Date: 2012-10-01

Variant appearance in text: rs157702
PubMed Link: 23028136
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: rs157702
PubMed Link: 20401335
Variant Present in the following documents:
  • Main text
  • gei-2-2009-023.pdf
View BVdb publication page



Sickle cell leg ulcers: associations with haemolysis and SNPs in Klotho, TEK and genes of the TGF-beta/BMP pathway.

British Journal Of Haematology
Nolan, Vikki G VG; Adewoye, Adeboye A; Baldwin, Clinton C; Wang, Ling L; Ma, Qianli Q; Wyszynski, Diego F DF; Farrell, John J JJ; Sebastiani, Paola P; Farrer, Lindsay A LA; Steinberg, Martin H MH
Publication Date: 2006-06

Variant appearance in text: rs157702
PubMed Link: 16681647
Variant Present in the following documents:
  • Main text
View BVdb publication page