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rs587782198

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587782198(-;-)
Make rs587782198(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108310307
GeneATM
is asnp
is mentioned by
dbSNPrs587782198
ebirs587782198
HLIrs587782198
Exacrs587782198
Varsomers587782198
Maprs587782198
PheGenIrs587782198
hapmaprs587782198
1000 genomesrs587782198
hgdprs587782198
ensemblrs587782198
gopubmedrs587782198
geneviewrs587782198
scholarrs587782198
googlers587782198
pharmgkbrs587782198
gwascentralrs587782198
openSNPrs587782198
23andMers587782198
23andMe allrs587782198
SNP Nexus

SNPshotrs587782198
SNPdbers587782198
MSV3drs587782198
GWAS Ctlgrs587782198
Max Magnitude0
ClinVar
Risk rs587782198(;)
Alt rs587782198(;)
Reference rs587782198(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108181034delA
CLNSRC
CLNACC RCV000130858.2,