PHLPP1 c.2960+10161T>C

Variant ID: 18-60597508-T-C

NM_194449.3(PHLPP1):c.2960+10161T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Search for inherited susceptibility to radiation-associated meningioma by genomewide SNP linkage disequilibrium mapping.

British Journal Of Cancer
Hosking, F J FJ; Feldman, D D; Bruchim, R R; Olver, B B; Lloyd, A A; Vijayakrishnan, J J; Flint-Richter, P P; Broderick, P P; Houlston, R S RS; Sadetzki, S S
Publication Date: 2011-03-15

Variant appearance in text: rs495005
PubMed Link: 21364586
Variant Present in the following documents:
  • Main text
  • bjc201161a.pdf
View BVdb publication page