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rs587781894

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781894(A;A)
Make rs587781894(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108365360
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587781894
ebirs587781894
HLIrs587781894
Exacrs587781894
Varsomers587781894
Maprs587781894
PheGenIrs587781894
hapmaprs587781894
1000 genomesrs587781894
hgdprs587781894
ensemblrs587781894
gopubmedrs587781894
geneviewrs587781894
scholarrs587781894
googlers587781894
pharmgkbrs587781894
gwascentralrs587781894
openSNPrs587781894
23andMers587781894
23andMe allrs587781894
SNP Nexus

SNPshotrs587781894
SNPdbers587781894
MSV3drs587781894
GWAS Ctlgrs587781894
Max Magnitude0
ClinVar
Risk rs587781894(A;A)
Alt rs587781894(A;A)
Reference rs587781894(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108236087G>A
CLNSRC
CLNACC RCV000130230.2, RCV000196159.1,