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rs587781597

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781597(A;A)
Make rs587781597(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108345829
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587781597
ebirs587781597
HLIrs587781597
Exacrs587781597
Varsomers587781597
Maprs587781597
PheGenIrs587781597
hapmaprs587781597
1000 genomesrs587781597
hgdprs587781597
ensemblrs587781597
gopubmedrs587781597
geneviewrs587781597
scholarrs587781597
googlers587781597
pharmgkbrs587781597
gwascentralrs587781597
openSNPrs587781597
23andMers587781597
23andMe allrs587781597
SNP Nexus

SNPshotrs587781597
SNPdbers587781597
MSV3drs587781597
GWAS Ctlgrs587781597
Max Magnitude0
ClinVar
Risk rs587781597(A;A)
Alt rs587781597(A;A)
Reference rs587781597(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108216556C>A
CLNSRC
CLNACC RCV000129661.2,