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rs587782847

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GAAACTGAAAG;GAAACTGAAAG) 0 common in clinvar
Make rs587782847(-;-)
Make rs587782847(-;AACTGAAAGGA)
Make rs587782847(AACTGAAAGGA;AACTGAAAGGA)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108365384
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587782847
dbSNP (old)rs587782847
ClinGenrs587782847
ebirs587782847
HLIrs587782847
Exacrs587782847
Gnomadrs587782847
Varsomers587782847
Maprs587782847
PheGenIrs587782847
Biobankrs587782847
1000 genomesrs587782847
hgdprs587782847
ensemblrs587782847
gopubmedrs587782847
geneviewrs587782847
scholarrs587782847
googlers587782847
pharmgkbrs587782847
gwascentralrs587782847
openSNPrs587782847
23andMers587782847
23andMe allrs587782847
SNP Nexus

SNPshotrs587782847
SNPdbers587782847
MSV3drs587782847
GWAS Ctlgrs587782847
Max Magnitude0
ClinVar
Risk rs587782847(-;-)
Alt rs587782847(-;-)
Reference Rs587782847(GAAACTGAAAG;GAAACTGAAAG)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108236111_108236121delAACTGAAAGGA
CLNSRC
CLNACC RCV000132441.2,