CTDSPL c.80-11131G>C

Variant ID: 3-37977417-G-C

NM_001008392.1(CTDSPL):c.80-11131G>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genome-wide study of copy number variation implicates multiple novel loci for schizophrenia risk in Han Chinese family trios.

Iscience
Wu, Xi X; Huai, Cong C; Shen, Lu L; Li, Mo M; Yang, Chao C; Zhang, Juan J; Chen, Luan L; Zhu, Wenli W; Fan, Lingzi L; Zhou, Wei W; Xing, Qinghe Q; He, Lin L; Wan, Chunling C; Qin, Shengying S
Publication Date: 2021-08-20

Variant appearance in text: rs9311168
PubMed Link: 34401673
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.

Bmc Medical Genetics
Seshadri, Sudha S; DeStefano, Anita L AL; Au, Rhoda R; Massaro, Joseph M JM; Beiser, Alexa S AS; Kelly-Hayes, Margaret M; Kase, Carlos S CS; D'Agostino, Ralph B RB; Decarli, Charles C; Atwood, Larry D LD; Wolf, Philip A PA
Publication Date: 2007-09-19

Variant appearance in text: rs9311168
PubMed Link: 17903297
Variant Present in the following documents:
  • Main text
  • 1471-2350-8-S1-S15.pdf
View BVdb publication page