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rs587780150

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780150(C;T)
Make rs587780150(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132589778
GeneRAD50
is asnp
is mentioned by
dbSNPrs587780150
dbSNP (classic)rs587780150
ClinGenrs587780150
ebirs587780150
HLIrs587780150
Exacrs587780150
Gnomadrs587780150
Varsomers587780150
LitVarrs587780150
Maprs587780150
PheGenIrs587780150
Biobankrs587780150
1000 genomesrs587780150
hgdprs587780150
ensemblrs587780150
geneviewrs587780150
scholarrs587780150
googlers587780150
pharmgkbrs587780150
gwascentralrs587780150
openSNPrs587780150
23andMers587780150
SNPshotrs587780150
SNPdbers587780150
MSV3drs587780150
GWAS Ctlgrs587780150
Max Magnitude0
ClinVar
Risk rs587780150(T;T)
Alt rs587780150(T;T)
Reference Rs587780150(C;C)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131925470C>T
CLNSRC
CLNACC RCV000115933.3, RCV000222369.1,