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rs587776551

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776551(A;A)
Make rs587776551(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position108281168
GeneATM
is asnp
is mentioned by
dbSNPrs587776551
ebirs587776551
HLIrs587776551
Exacrs587776551
Varsomers587776551
Maprs587776551
PheGenIrs587776551
hapmaprs587776551
1000 genomesrs587776551
hgdprs587776551
ensemblrs587776551
gopubmedrs587776551
geneviewrs587776551
scholarrs587776551
googlers587776551
pharmgkbrs587776551
gwascentralrs587776551
openSNPrs587776551
23andMers587776551
23andMe allrs587776551
SNP Nexus

SNPshotrs587776551
SNPdbers587776551
MSV3drs587776551
GWAS Ctlgrs587776551
Max Magnitude0
ClinVar
Risk rs587776551(A;A)
Alt rs587776551(A;A)
Reference rs587776551(G;G)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108151895G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003174.4, RCV000165646.1, RCV000236731.1,