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rs776276760

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs776276760(C;G)
Make rs776276760(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132588882
GeneRAD50
is asnp
is mentioned by
dbSNPrs776276760
ebirs776276760
HLIrs776276760
Exacrs776276760
Varsomers776276760
Maprs776276760
PheGenIrs776276760
hapmaprs776276760
1000 genomesrs776276760
hgdprs776276760
ensemblrs776276760
gopubmedrs776276760
geneviewrs776276760
scholarrs776276760
googlers776276760
pharmgkbrs776276760
gwascentralrs776276760
openSNPrs776276760
23andMers776276760
23andMe allrs776276760
SNP Nexus

SNPshotrs776276760
SNPdbers776276760
MSV3drs776276760
GWAS Ctlgrs776276760
Max Magnitude0
ClinVar
Risk rs776276760(G;G)
Alt rs776276760(G;G)
Reference rs776276760(C;C)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131924574C>G
CLNSRC
CLNACC RCV000234702.1,