PTPRQ c.5736+513T>C

Variant ID: 12-81052353-T-C

NM_001145026.2(PTPRQ):c.5736+513T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis.

European Journal Of Human Genetics : Ejhg
Simpson, Claire L CL; Cropp, Cheryl D CD; Wahlfors, Tiina T; George, Asha A; Jones, Marypat S MS; Harper, Ursula U; Ponciano-Jackson, Damaris D; Tammela, Teuvo T; Schleutker, Johanna J; Bailey-Wilson, Joan E JE
Publication Date: 2013-04

Variant appearance in text: rs1163016
PubMed Link: 22948022
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide linkage scan for prostate cancer susceptibility in Finland: evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21-q22.

International Journal Of Cancer
Cropp, Cheryl D CD; Simpson, Claire L CL; Wahlfors, Tiina T; Ha, Nati N; George, Asha A; Jones, MaryPat S MS; Harper, Ursula U; Ponciano-Jackson, Damaris D; Green, Tiffany A TA; Tammela, Teuvo L J TL; Bailey-Wilson, Joan J; Schleutker, Johanna J
Publication Date: 2011-11-15

Variant appearance in text: rs1163016
PubMed Link: 21207418
Variant Present in the following documents:
  • Main text
View BVdb publication page