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rs587782652

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782652(C;C)
Make rs587782652(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108335105
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587782652
ebirs587782652
HLIrs587782652
Exacrs587782652
Varsomers587782652
Maprs587782652
PheGenIrs587782652
hapmaprs587782652
1000 genomesrs587782652
hgdprs587782652
ensemblrs587782652
gopubmedrs587782652
geneviewrs587782652
scholarrs587782652
googlers587782652
pharmgkbrs587782652
gwascentralrs587782652
openSNPrs587782652
23andMers587782652
23andMe allrs587782652
SNP Nexus

SNPshotrs587782652
SNPdbers587782652
MSV3drs587782652
GWAS Ctlgrs587782652
Max Magnitude0
ClinVar
Risk rs587782652(C;C)
Alt rs587782652(C;C)
Reference rs587782652(T;T)
Significance Other
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108205832T>C
CLNSRC
CLNACC RCV000132066.5, RCV000169105.3, RCV000212079.2,