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rs587782090

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782090(G;T)
Make rs587782090(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132587942
GeneRAD50
is asnp
is mentioned by
dbSNPrs587782090
ebirs587782090
HLIrs587782090
Exacrs587782090
Varsomers587782090
Maprs587782090
PheGenIrs587782090
hapmaprs587782090
1000 genomesrs587782090
hgdprs587782090
ensemblrs587782090
gopubmedrs587782090
geneviewrs587782090
scholarrs587782090
googlers587782090
pharmgkbrs587782090
gwascentralrs587782090
openSNPrs587782090
23andMers587782090
23andMe allrs587782090
SNP Nexus

SNPshotrs587782090
SNPdbers587782090
MSV3drs587782090
GWAS Ctlgrs587782090
Max Magnitude0
ClinVar
Risk rs587782090(T;T)
Alt rs587782090(T;T)
Reference rs587782090(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131923634G>T
CLNSRC
CLNACC RCV000130597.2,