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rs4809324

From SNPedia

Orientationplus
Stabilizedplus
Make rs4809324(C;C)
Make rs4809324(C;T)
Make rs4809324(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position63686867
GenePLEKHJ1, RTEL1
is asnp
is mentioned by
dbSNPrs4809324
ebirs4809324
HLIrs4809324
Exacrs4809324
Varsomers4809324
Maprs4809324
PheGenIrs4809324
hapmaprs4809324
1000 genomesrs4809324
hgdprs4809324
ensemblrs4809324
gopubmedrs4809324
geneviewrs4809324
scholarrs4809324
googlers4809324
pharmgkbrs4809324
gwascentralrs4809324
openSNPrs4809324
23andMers4809324
23andMe allrs4809324
SNP Nexus

SNPshotrs4809324
SNPdbers4809324
MSV3drs4809324
GWAS Ctlgrs4809324
GMAF0.1125
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19578366OA-icon.png]
Trait Glioma (high-grade)
Title Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility
Risk Allele C
P-val 2E-9
Odds Ratio 1.60 [1.37-1.87]
OMIM613031
Desc
Variant
Relatedalso


GET Evidence
rs4809324
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.132812
summary



[PMID 26014354] CCDC26, CDKN2BAS, RTEL1 and TERT Polymorphisms in pediatric brain tumor susceptibility