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rs587782660

From SNPedia

Orientationplus
Geno Mag Summary
(CCTC;CCTC) 0 common in clinvar
Make rs587782660(-;-)
Make rs587782660(-;CCTC)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108244842
GeneATM
is asnp
is mentioned by
dbSNPrs587782660
ebirs587782660
HLIrs587782660
Exacrs587782660
Varsomers587782660
Maprs587782660
PheGenIrs587782660
hapmaprs587782660
1000 genomesrs587782660
hgdprs587782660
ensemblrs587782660
gopubmedrs587782660
geneviewrs587782660
scholarrs587782660
googlers587782660
pharmgkbrs587782660
gwascentralrs587782660
openSNPrs587782660
23andMers587782660
23andMe allrs587782660
SNP Nexus

SNPshotrs587782660
SNPdbers587782660
MSV3drs587782660
GWAS Ctlgrs587782660
Max Magnitude0
ClinVar
Risk rs587782660(;)
Alt rs587782660(;)
Reference rs587782660(CCTC;CCTC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108115569_108115572delCCTC
CLNSRC
CLNACC RCV000132076.2,