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rs397507177

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507177(C;T)
Make rs397507177(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position132608717
GeneRAD50
is asnp
is mentioned by
dbSNPrs397507177
ebirs397507177
HLIrs397507177
Exacrs397507177
Varsomers397507177
Maprs397507177
PheGenIrs397507177
hapmaprs397507177
1000 genomesrs397507177
hgdprs397507177
ensemblrs397507177
gopubmedrs397507177
geneviewrs397507177
scholarrs397507177
googlers397507177
pharmgkbrs397507177
gwascentralrs397507177
openSNPrs397507177
23andMers397507177
23andMe allrs397507177
SNP Nexus

SNPshotrs397507177
SNPdbers397507177
MSV3drs397507177
GWAS Ctlgrs397507177
Max Magnitude0
ClinVar
Risk rs397507177(T;T)
Alt rs397507177(T;T)
Reference rs397507177(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.131944409C>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000030957.3,