SORCS1 c.727-17171G>C

Variant ID: 10-108553621-C-G

NM_052918.4(SORCS1):c.727-17171G>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10.

Human Mutation
Liang, Xueying X; Slifer, Michael M; Martin, Eden R ER; Schnetz-Boutaud, Nathalie N; Bartlett, Jackie J; Anderson, Brent B; Züchner, Stephan S; Gwirtsman, Harry H; Gilbert, John R JR; Pericak-Vance, Margaret A MA; Haines, Jonathan L JL
Publication Date: 2009-03

Variant appearance in text: rs11193054
PubMed Link: 19241460
Variant Present in the following documents:
  • Main text
View BVdb publication page