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rs587781454

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781454(-;-)
Make rs587781454(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132595768
GeneRAD50
is asnp
is mentioned by
dbSNPrs587781454
ebirs587781454
HLIrs587781454
Exacrs587781454
Varsomers587781454
Maprs587781454
PheGenIrs587781454
hapmaprs587781454
1000 genomesrs587781454
hgdprs587781454
ensemblrs587781454
gopubmedrs587781454
geneviewrs587781454
scholarrs587781454
googlers587781454
pharmgkbrs587781454
gwascentralrs587781454
openSNPrs587781454
23andMers587781454
23andMe allrs587781454
SNP Nexus

SNPshotrs587781454
SNPdbers587781454
MSV3drs587781454
GWAS Ctlgrs587781454
Max Magnitude0
ClinVar
Risk rs587781454(AA,AT;AA,AT)
Alt rs587781454(AA,AT;AA,AT)
Reference rs587781454(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131931460dupA
CLNSRC
CLNACC RCV000129381.5,