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rs587782863

From SNPedia

Orientationplus
Geno Mag Summary
(AAAAA;AAAAA) 0 common in clinvar
Make rs587782863(-;-)
Make rs587782863(-;AAAAA)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108289724
GeneATM
is asnp
is mentioned by
dbSNPrs587782863
ebirs587782863
HLIrs587782863
Exacrs587782863
Varsomers587782863
Maprs587782863
PheGenIrs587782863
hapmaprs587782863
1000 genomesrs587782863
hgdprs587782863
ensemblrs587782863
gopubmedrs587782863
geneviewrs587782863
scholarrs587782863
googlers587782863
pharmgkbrs587782863
gwascentralrs587782863
openSNPrs587782863
23andMers587782863
23andMe allrs587782863
SNP Nexus

SNPshotrs587782863
SNPdbers587782863
MSV3drs587782863
GWAS Ctlgrs587782863
Max Magnitude0
ClinVar
Risk rs587782863(;)
Alt rs587782863(;)
Reference rs587782863(AAAAA;AAAAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108160451_108160455delAAAAA
CLNSRC
CLNACC RCV000132482.2,