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rs587781727

From SNPedia

Orientationplus
Geno Mag Summary
(AAGAA;AAGAA) 0 common in clinvar
Make rs587781727(-;-)
Make rs587781727(-;AAAAG)
Make rs587781727(AAAAG;AAAAG)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108310290
GeneATM
is asnp
is mentioned by
dbSNPrs587781727
ebirs587781727
HLIrs587781727
Exacrs587781727
Varsomers587781727
Maprs587781727
PheGenIrs587781727
hapmaprs587781727
1000 genomesrs587781727
hgdprs587781727
ensemblrs587781727
gopubmedrs587781727
geneviewrs587781727
scholarrs587781727
googlers587781727
pharmgkbrs587781727
gwascentralrs587781727
openSNPrs587781727
23andMers587781727
23andMe allrs587781727
SNP Nexus

SNPshotrs587781727
SNPdbers587781727
MSV3drs587781727
GWAS Ctlgrs587781727
Max Magnitude0
ClinVar
Risk rs587781727(;)
Alt rs587781727(;)
Reference rs587781727(AAGAA;AAGAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108181017_108181021delAAAAG
CLNSRC
CLNACC RCV000129915.2,