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rs878854797

From SNPedia

Orientationplus
Geno Mag Summary
(AGAAAGAA;AGAAAGAA) 0 common in clinvar
Make rs878854797(AGAAAGAA;T)
Make rs878854797(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132618171
GeneRAD50
is asnp
is mentioned by
dbSNPrs878854797
ebirs878854797
HLIrs878854797
Exacrs878854797
Varsomers878854797
Maprs878854797
PheGenIrs878854797
hapmaprs878854797
1000 genomesrs878854797
hgdprs878854797
ensemblrs878854797
gopubmedrs878854797
geneviewrs878854797
scholarrs878854797
googlers878854797
pharmgkbrs878854797
gwascentralrs878854797
openSNPrs878854797
23andMers878854797
23andMe allrs878854797
SNP Nexus

SNPshotrs878854797
SNPdbers878854797
MSV3drs878854797
GWAS Ctlgrs878854797
Max Magnitude0
ClinVar
Risk rs878854797(T;T)
Alt rs878854797(T;T)
Reference rs878854797(AGAAAGAA;AGAAAGAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131953863_131953870delAGAAAGAAinsT
CLNSRC
CLNACC RCV000232037.1,