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rs587781656

From SNPedia

Orientationplus
Geno Mag Summary
(AAACC;AAACC) 0 common in clinvar
Make rs587781656(-;-)
Make rs587781656(-;AACCA)
Make rs587781656(AACCA;AACCA)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108271137
GeneATM
is asnp
is mentioned by
dbSNPrs587781656
ebirs587781656
HLIrs587781656
Exacrs587781656
Varsomers587781656
Maprs587781656
PheGenIrs587781656
hapmaprs587781656
1000 genomesrs587781656
hgdprs587781656
ensemblrs587781656
gopubmedrs587781656
geneviewrs587781656
scholarrs587781656
googlers587781656
pharmgkbrs587781656
gwascentralrs587781656
openSNPrs587781656
23andMers587781656
23andMe allrs587781656
SNP Nexus

SNPshotrs587781656
SNPdbers587781656
MSV3drs587781656
GWAS Ctlgrs587781656
Max Magnitude0
ClinVar
Risk rs587781656(;)
Alt rs587781656(;)
Reference rs587781656(AAACC;AAACC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108141864_108141868delAACCA
CLNSRC
CLNACC RCV000129795.2,