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rs587781754

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781754(-;-)
Make rs587781754(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108297315
GeneATM
is asnp
is mentioned by
dbSNPrs587781754
ebirs587781754
HLIrs587781754
Exacrs587781754
Varsomers587781754
Maprs587781754
PheGenIrs587781754
hapmaprs587781754
1000 genomesrs587781754
hgdprs587781754
ensemblrs587781754
gopubmedrs587781754
geneviewrs587781754
scholarrs587781754
googlers587781754
pharmgkbrs587781754
gwascentralrs587781754
openSNPrs587781754
23andMers587781754
23andMe allrs587781754
SNP Nexus

SNPshotrs587781754
SNPdbers587781754
MSV3drs587781754
GWAS Ctlgrs587781754
Max Magnitude0
ClinVar
Risk rs587781754(;)
Alt rs587781754(;)
Reference rs587781754(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108168042delA
CLNSRC
CLNACC RCV000129960.2,