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rs200196781

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200196781(A;A)
Make rs200196781(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position108284474
GeneATM
is asnp
is mentioned by
dbSNPrs200196781
ebirs200196781
HLIrs200196781
Exacrs200196781
Varsomers200196781
Maprs200196781
PheGenIrs200196781
hapmaprs200196781
1000 genomesrs200196781
hgdprs200196781
ensemblrs200196781
gopubmedrs200196781
geneviewrs200196781
scholarrs200196781
googlers200196781
pharmgkbrs200196781
gwascentralrs200196781
openSNPrs200196781
23andMers200196781
23andMe allrs200196781
SNP Nexus

SNPshotrs200196781
SNPdbers200196781
MSV3drs200196781
GWAS Ctlgrs200196781
Max Magnitude0
ClinVar
Risk rs200196781(A;A)
Alt rs200196781(A;A)
Reference rs200196781(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108155201G>A
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000129961.2, RCV000228950.1,