RYR3 c.52-10709A>G

Variant ID: 15-33754911-A-G

NM_001036.3(RYR3):c.52-10709A>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Genetic Variants behind Cardiovascular Diseases and Dementia.

Genes
Ho, Wei-Min WM; Wu, Yah-Yuan YY; Chen, Yi-Chun YC
Publication Date: 2020-12-18

Variant appearance in text: rs2033610
PubMed Link: 33352859
Variant Present in the following documents:
  • Main text
  • genes-11-01514.pdf
View BVdb publication page



Genome-wide linkage analyses of hereditary prostate cancer families with colon cancer provide further evidence for a susceptibility locus on 15q11-q14.

European Journal Of Human Genetics : Ejhg
Fitzgerald, Liesel M LM; McDonnell, Shannon K SK; Carlson, Erin E EE; Langeberg, Wendy W; McIntosh, Laura M LM; Deutsch, Kerry K; Ostrander, Elaine A EA; Schaid, Daniel J DJ; Stanford, Janet L JL
Publication Date: 2010-10

Variant appearance in text: rs2033610
PubMed Link: 20407467
Variant Present in the following documents:
  • Main text
View BVdb publication page



Dense genome-wide SNP linkage scan in 301 hereditary prostate cancer families identifies multiple regions with suggestive evidence for linkage.

Human Molecular Genetics
Stanford, Janet L JL; FitzGerald, Liesel M LM; McDonnell, Shannon K SK; Carlson, Erin E EE; McIntosh, Laura M LM; Deutsch, Kerry K; Hood, Lee L; Ostrander, Elaine A EA; Schaid, Daniel J DJ
Publication Date: 2009-05-15

Variant appearance in text: rs2033610
PubMed Link: 19251732
Variant Present in the following documents:
  • Main text
View BVdb publication page