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rs587782488

From SNPedia

Orientationplus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
Make rs587782488(-;-)
Make rs587782488(-;AAAG)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132609340
GeneRAD50
is asnp
is mentioned by
dbSNPrs587782488
ebirs587782488
HLIrs587782488
Exacrs587782488
Varsomers587782488
Maprs587782488
PheGenIrs587782488
hapmaprs587782488
1000 genomesrs587782488
hgdprs587782488
ensemblrs587782488
gopubmedrs587782488
geneviewrs587782488
scholarrs587782488
googlers587782488
pharmgkbrs587782488
gwascentralrs587782488
openSNPrs587782488
23andMers587782488
23andMe allrs587782488
SNP Nexus

SNPshotrs587782488
SNPdbers587782488
MSV3drs587782488
GWAS Ctlgrs587782488
Max Magnitude0
ClinVar
Risk rs587782488(;)
Alt rs587782488(;)
Reference rs587782488(AAAG;AAAG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131945035_131945038delGAAA
CLNSRC
CLNACC RCV000115951.3,