SDCCAG8 c.2113-1031T>C

Variant ID: 1-243662027-T-C

NM_006642.3(SDCCAG8):c.2113-1031T>C

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Multiple SNP Set Analysis for Genome-Wide Association Studies Through Bayesian Latent Variable Selection.

Genetic Epidemiology
Lu, Zhao-Hua ZH; Zhu, Hongtu H; Knickmeyer, Rebecca C RC; Sullivan, Patrick F PF; Williams, Stephanie N SN; Zou, Fei F; ,
Publication Date: 2015-12

Variant appearance in text: rs9428576
PubMed Link: 26515609
Variant Present in the following documents:
  • Main text
View BVdb publication page