IDE c.1060+151C>A

Variant ID: 10-94268334-G-T

NM_004969.3(IDE):c.1060+151C>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs1832196
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



Evidence that the gene encoding insulin degrading enzyme influences human lifespan.

Human Molecular Genetics
Hong, Mun-Gwan MG; Reynolds, Chandra C; Gatz, Margaret M; Johansson, Boo B; Palmer, Jennifer C JC; Gu, Harvest F HF; Blennow, Kaj K; Kehoe, Patrick G PG; de Faire, Ulf U; Pedersen, Nancy L NL; Prince, Jonathan A JA
Publication Date: 2008-08-01

Variant appearance in text: rs1832196
PubMed Link: 18448515
Variant Present in the following documents:
  • Main text
View BVdb publication page



Confronting complexity in late-onset Alzheimer disease: application of two-stage analysis approach addressing heterogeneity and epistasis.

Genetic Epidemiology
Thornton-Wells, Tricia A TA; Moore, Jason H JH; Martin, Eden R ER; Pericak-Vance, Margaret A MA; Haines, Jonathan L JL
Publication Date: 2008-04

Variant appearance in text: rs1832196
PubMed Link: 18076107
Variant Present in the following documents:
  • Main text
View BVdb publication page