IGF1R c.641-79288T>C

Variant ID: 15-99355266-T-C

NM_000875.3(IGF1R):c.641-79288T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


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: rs6598554
PubMed Link: 19251732
Variant Present in the following documents:
  • Main text
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