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rs587780154

From SNPedia

Orientationplus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
Make rs587780154(-;-)
Make rs587780154(-;GAAA)
Make rs587780154(GAAA;GAAA)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132609343
GeneRAD50
is asnp
is mentioned by
dbSNPrs587780154
ebirs587780154
HLIrs587780154
Exacrs587780154
Varsomers587780154
Maprs587780154
PheGenIrs587780154
hapmaprs587780154
1000 genomesrs587780154
hgdprs587780154
ensemblrs587780154
gopubmedrs587780154
geneviewrs587780154
scholarrs587780154
googlers587780154
pharmgkbrs587780154
gwascentralrs587780154
openSNPrs587780154
23andMers587780154
23andMe allrs587780154
SNP Nexus

SNPshotrs587780154
SNPdbers587780154
MSV3drs587780154
GWAS Ctlgrs587780154
Max Magnitude0
ClinVar
Risk rs587780154(;)
Alt rs587780154(;)
Reference rs587780154(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,