CALCRL c.501-1917G>A

Variant ID: 2-188230146-C-T

NM_005795.5(CALCRL):c.501-1917G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.

Nature Genetics
Weinhold, Niels N; Johnson, David C DC; Chubb, Daniel D; Chen, Bowang B; Försti, Asta A; Hosking, Fay J FJ; Broderick, Peter P; Ma, Yussanne P YP; Dobbins, Sara E SE; Hose, Dirk D; Walker, Brian A BA; Davies, Faith E FE; Kaiser, Martin F MF; Li, Ni L NL; Gregory, Walter A WA; Jackson, Graham H GH; Witzens-Harig, Mathias M; Neben, Kai K; Hoffmann, Per P; Nöthen, Markus M MM; Mühleisen, Thomas W TW; Eisele, Lewin L; Ross, Fiona M FM; Jauch, Anna A; Goldschmidt, Hartmut H; Houlston, Richard S RS; Morgan, Gareth J GJ; Hemminki, Kari K
Publication Date: 2013-05

Variant appearance in text: rs3771089
PubMed Link: 23502783
Variant Present in the following documents:
  • NIHMS53125-supplement-1.pdf
View BVdb publication page