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rs764122619

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs764122619(C;C)
Make rs764122619(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132580068
GeneRAD50
is asnp
is mentioned by
dbSNPrs764122619
ebirs764122619
HLIrs764122619
Exacrs764122619
Varsomers764122619
Maprs764122619
PheGenIrs764122619
hapmaprs764122619
1000 genomesrs764122619
hgdprs764122619
ensemblrs764122619
gopubmedrs764122619
geneviewrs764122619
scholarrs764122619
googlers764122619
pharmgkbrs764122619
gwascentralrs764122619
openSNPrs764122619
23andMers764122619
23andMe allrs764122619
SNP Nexus

SNPshotrs764122619
SNPdbers764122619
MSV3drs764122619
GWAS Ctlgrs764122619
Max Magnitude0
ClinVar
Risk rs764122619(C;C)
Alt rs764122619(C;C)
Reference rs764122619(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131915760T>C
CLNSRC
CLNACC RCV000164601.2,