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rs587782078

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782078(A;A)
Make rs587782078(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132595045
GeneRAD50
is asnp
is mentioned by
dbSNPrs587782078
ebirs587782078
HLIrs587782078
Exacrs587782078
Varsomers587782078
Maprs587782078
PheGenIrs587782078
hapmaprs587782078
1000 genomesrs587782078
hgdprs587782078
ensemblrs587782078
gopubmedrs587782078
geneviewrs587782078
scholarrs587782078
googlers587782078
pharmgkbrs587782078
gwascentralrs587782078
openSNPrs587782078
23andMers587782078
23andMe allrs587782078
SNP Nexus

SNPshotrs587782078
SNPdbers587782078
MSV3drs587782078
GWAS Ctlgrs587782078
Max Magnitude0
ClinVar
Risk rs587782078(A;A)
Alt rs587782078(A;A)
Reference rs587782078(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131930737G>A
CLNSRC
CLNACC RCV000130574.2,