Have questions? Visit https://www.reddit.com/r/SNPedia

rs587782543

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587782543(-;-)
Make rs587782543(-;A)
Make rs587782543(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132591958
GeneRAD50
is asnp
is mentioned by
dbSNPrs587782543
ebirs587782543
HLIrs587782543
Exacrs587782543
Varsomers587782543
Maprs587782543
PheGenIrs587782543
hapmaprs587782543
1000 genomesrs587782543
hgdprs587782543
ensemblrs587782543
gopubmedrs587782543
geneviewrs587782543
scholarrs587782543
googlers587782543
pharmgkbrs587782543
gwascentralrs587782543
openSNPrs587782543
23andMers587782543
23andMe allrs587782543
SNP Nexus

SNPshotrs587782543
SNPdbers587782543
MSV3drs587782543
GWAS Ctlgrs587782543
Max Magnitude0
ClinVar
Risk rs587782543(A;A)
Alt rs587782543(A;A)
Reference rs587782543(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131927650dupA
CLNSRC
CLNACC RCV000131751.2,