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rs776395588

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs776395588(C;C)
Make rs776395588(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132604038
GeneRAD50
is asnp
is mentioned by
dbSNPrs776395588
ebirs776395588
HLIrs776395588
Exacrs776395588
Varsomers776395588
Maprs776395588
PheGenIrs776395588
hapmaprs776395588
1000 genomesrs776395588
hgdprs776395588
ensemblrs776395588
gopubmedrs776395588
geneviewrs776395588
scholarrs776395588
googlers776395588
pharmgkbrs776395588
gwascentralrs776395588
openSNPrs776395588
23andMers776395588
23andMe allrs776395588
SNP Nexus

SNPshotrs776395588
SNPdbers776395588
MSV3drs776395588
GWAS Ctlgrs776395588
Max Magnitude0
ClinVar
Risk rs776395588(A,C;A,C)
Alt rs776395588(A,C;A,C)
Reference rs776395588(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131939730T>A
CLNSRC
CLNACC RCV000164879.1,