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rs587781576

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781576(C;T)
Make rs587781576(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132579953
GeneRAD50
is asnp
is mentioned by
dbSNPrs587781576
ebirs587781576
HLIrs587781576
Exacrs587781576
Varsomers587781576
Maprs587781576
PheGenIrs587781576
hapmaprs587781576
1000 genomesrs587781576
hgdprs587781576
ensemblrs587781576
gopubmedrs587781576
geneviewrs587781576
scholarrs587781576
googlers587781576
pharmgkbrs587781576
gwascentralrs587781576
openSNPrs587781576
23andMers587781576
23andMe allrs587781576
SNP Nexus

SNPshotrs587781576
SNPdbers587781576
MSV3drs587781576
GWAS Ctlgrs587781576
Max Magnitude0
ClinVar
Risk rs587781576(T;T)
Alt rs587781576(T;T)
Reference rs587781576(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131915645C>T
CLNSRC
CLNACC RCV000129612.2,