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rs587780155

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGAC;AGAC) 0 common in clinvar
(CAGA;CAGA) 0 common in clinvar
(I;I) 0 common genotype
Make rs587780155(-;-)
Make rs587780155(-;CAGA)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132575889
GeneRAD50
is asnp
is mentioned by
dbSNPrs587780155
dbSNP (classic)rs587780155
ClinGenrs587780155
ebirs587780155
HLIrs587780155
Exacrs587780155
Gnomadrs587780155
Varsomers587780155
LitVarrs587780155
Maprs587780155
PheGenIrs587780155
Biobankrs587780155
1000 genomesrs587780155
hgdprs587780155
ensemblrs587780155
geneviewrs587780155
scholarrs587780155
googlers587780155
pharmgkbrs587780155
gwascentralrs587780155
openSNPrs587780155
23andMers587780155
SNPshotrs587780155
SNPdbers587780155
MSV3drs587780155
GWAS Ctlgrs587780155
Max Magnitude0
ClinVar
Risk rs587780155(-;-) Rs587780155(AGAC;AGAC)
Alt rs587780155(-;-) Rs587780155(AGAC;AGAC)
Reference Rs587780155(CAGA;CAGA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131911581_131911584delCAGA
CLNSRC
CLNACC RCV000115954.5,