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rs587776549

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATC;ATC) 0 common in clinvar
Make rs587776549(ATC;TGAT)
Make rs587776549(TGAT;TGAT)
ReferenceGRCh38 38.1/142
Chromosome11
Position108272813
GeneATM
is asnp
is mentioned by
dbSNPrs587776549
dbSNP (old)rs587776549
ClinGenrs587776549
ebirs587776549
HLIrs587776549
Exacrs587776549
Gnomadrs587776549
Varsomers587776549
Maprs587776549
PheGenIrs587776549
Biobankrs587776549
1000 genomesrs587776549
hgdprs587776549
ensemblrs587776549
gopubmedrs587776549
geneviewrs587776549
scholarrs587776549
googlers587776549
pharmgkbrs587776549
gwascentralrs587776549
openSNPrs587776549
23andMers587776549
23andMe allrs587776549
SNP Nexus

SNPshotrs587776549
SNPdbers587776549
MSV3drs587776549
GWAS Ctlgrs587776549
Max Magnitude0
ClinVar
Risk rs587776549(TGAT;TGAT)
Alt rs587776549(TGAT;TGAT)
Reference Rs587776549(ATC;ATC)
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.108143540_108143542delATCinsTGAT
CLNSRC OMIM Allelic Variant
CLNACC RCV000003172.6, RCV000159638.5, RCV000235102.2,