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rs587781347

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs587781347(-;-)
Make rs587781347(-;AA)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108250867
GeneATM
is asnp
is mentioned by
dbSNPrs587781347
ebirs587781347
HLIrs587781347
Exacrs587781347
Varsomers587781347
Maprs587781347
PheGenIrs587781347
hapmaprs587781347
1000 genomesrs587781347
hgdprs587781347
ensemblrs587781347
gopubmedrs587781347
geneviewrs587781347
scholarrs587781347
googlers587781347
pharmgkbrs587781347
gwascentralrs587781347
openSNPrs587781347
23andMers587781347
23andMe allrs587781347
SNP Nexus

SNPshotrs587781347
SNPdbers587781347
MSV3drs587781347
GWAS Ctlgrs587781347
Max Magnitude0
ClinVar
Risk rs587781347(;)
Alt rs587781347(;)
Reference rs587781347(AA;AA)
Significance Other
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108121594_108121595delAA
CLNSRC
CLNACC RCV000129125.2, RCV000169588.3, RCV000236583.1,