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rs587781742

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781742(G;T)
Make rs587781742(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132594868
GeneRAD50
is asnp
is mentioned by
dbSNPrs587781742
ebirs587781742
HLIrs587781742
Exacrs587781742
Varsomers587781742
Maprs587781742
PheGenIrs587781742
hapmaprs587781742
1000 genomesrs587781742
hgdprs587781742
ensemblrs587781742
gopubmedrs587781742
geneviewrs587781742
scholarrs587781742
googlers587781742
pharmgkbrs587781742
gwascentralrs587781742
openSNPrs587781742
23andMers587781742
23andMe allrs587781742
SNP Nexus

SNPshotrs587781742
SNPdbers587781742
MSV3drs587781742
GWAS Ctlgrs587781742
Max Magnitude0
ClinVar
Risk rs587781742(A,T;A,T)
Alt rs587781742(A,T;A,T)
Reference rs587781742(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.131930560G>T
CLNSRC
CLNACC RCV000129946.2,