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rs587781904

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781904(A;A)
Make rs587781904(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132595033
GeneRAD50
is asnp
is mentioned by
dbSNPrs587781904
ebirs587781904
HLIrs587781904
Exacrs587781904
Varsomers587781904
Maprs587781904
PheGenIrs587781904
hapmaprs587781904
1000 genomesrs587781904
hgdprs587781904
ensemblrs587781904
gopubmedrs587781904
geneviewrs587781904
scholarrs587781904
googlers587781904
pharmgkbrs587781904
gwascentralrs587781904
openSNPrs587781904
23andMers587781904
23andMe allrs587781904
SNP Nexus

SNPshotrs587781904
SNPdbers587781904
MSV3drs587781904
GWAS Ctlgrs587781904
Max Magnitude0
ClinVar
Risk rs587781904(A;A)
Alt rs587781904(A;A)
Reference rs587781904(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.131930725C>A
CLNSRC
CLNACC RCV000130243.3,