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rs587782292

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782292(C;T)
Make rs587782292(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108365359
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587782292
ebirs587782292
HLIrs587782292
Exacrs587782292
Varsomers587782292
Maprs587782292
PheGenIrs587782292
hapmaprs587782292
1000 genomesrs587782292
hgdprs587782292
ensemblrs587782292
gopubmedrs587782292
geneviewrs587782292
scholarrs587782292
googlers587782292
pharmgkbrs587782292
gwascentralrs587782292
openSNPrs587782292
23andMers587782292
23andMe allrs587782292
SNP Nexus

SNPshotrs587782292
SNPdbers587782292
MSV3drs587782292
GWAS Ctlgrs587782292
Max Magnitude0
ClinVar
Risk rs587782292(T;T)
Alt rs587782292(T;T)
Reference rs587782292(C;C)
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.108236086C>T
CLNSRC
CLNACC RCV000131173.4, RCV000169274.2, RCV000212096.1,