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rs373428259

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs373428259(C;T)
Make rs373428259(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132588872
GeneRAD50
is asnp
is mentioned by
dbSNPrs373428259
ebirs373428259
HLIrs373428259
Exacrs373428259
Varsomers373428259
Maprs373428259
PheGenIrs373428259
hapmaprs373428259
1000 genomesrs373428259
hgdprs373428259
ensemblrs373428259
gopubmedrs373428259
geneviewrs373428259
scholarrs373428259
googlers373428259
pharmgkbrs373428259
gwascentralrs373428259
openSNPrs373428259
23andMers373428259
23andMe allrs373428259
SNP Nexus

SNPshotrs373428259
SNPdbers373428259
MSV3drs373428259
GWAS Ctlgrs373428259
Max Magnitude0
ClinVar
Risk rs373428259(A,G,T;A,G,T)
Alt rs373428259(A,G,T;A,G,T)
Reference rs373428259(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131924564C>T
CLNSRC
CLNACC RCV000163726.1,