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rs587780153

From SNPedia

Orientationplus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
Make rs587780153(-;-)
Make rs587780153(-;GAAA)
Make rs587780153(GAAA;GAAA)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132609289
GeneRAD50
is asnp
is mentioned by
dbSNPrs587780153
ebirs587780153
HLIrs587780153
Exacrs587780153
Varsomers587780153
Maprs587780153
PheGenIrs587780153
hapmaprs587780153
1000 genomesrs587780153
hgdprs587780153
ensemblrs587780153
gopubmedrs587780153
geneviewrs587780153
scholarrs587780153
googlers587780153
pharmgkbrs587780153
gwascentralrs587780153
openSNPrs587780153
23andMers587780153
23andMe allrs587780153
SNP Nexus

SNPshotrs587780153
SNPdbers587780153
MSV3drs587780153
GWAS Ctlgrs587780153
Max Magnitude0
ClinVar
Risk rs587780153(;)
Alt rs587780153(;)
Reference rs587780153(AAAG;AAAG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.131944981_131944984delGAAA
CLNSRC
CLNACC RCV000115950.2, RCV000218000.1,