FRK c.345-2418G>A

Variant ID: 6-116327579-C-T

NM_002031.2(FRK):c.345-2418G>A

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:

MegaSNPHunter: a learning approach to detect disease predisposition SNPs and high level interactions in genome wide association study.

Bmc Bioinformatics
Wan, Xiang X; Yang, Can C; Yang, Qiang Q; Xue, Hong H; Tang, Nelson L S NL; Yu, Weichuan W
Publication Date: 2009-01-09

Variant appearance in text: rs9387380
PubMed Link: 19134182
Variant Present in the following documents:
  • Main text
  • 1471-2105-10-13.pdf
View BVdb publication page