CSMD1 c.1010-20507A>G

Variant ID: 8-3494826-T-C

NM_033225.5(CSMD1):c.1010-20507A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome-wide screen for universal individual identification SNPs based on the HapMap and 1000 Genomes databases.

Scientific Reports
Huang, Erwen E; Liu, Changhui C; Zheng, Jingjing J; Han, Xiaolong X; Du, Weian W; Huang, Yuanjian Y; Li, Chengshi C; Wang, Xiaoguang X; Tong, Dayue D; Ou, Xueling X; Sun, Hongyu H; Zeng, Zhaoshu Z; Liu, Chao C
Publication Date: 2018-04-03

Variant appearance in text: rs4469483
PubMed Link: 29615764
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_23888.pdf
View BVdb publication page