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rs55861249

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs55861249(C;T)
Make rs55861249(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position108227806
GeneATM
is asnp
is mentioned by
dbSNPrs55861249
ebirs55861249
HLIrs55861249
Exacrs55861249
Varsomers55861249
Maprs55861249
PheGenIrs55861249
hapmaprs55861249
1000 genomesrs55861249
hgdprs55861249
ensemblrs55861249
gopubmedrs55861249
geneviewrs55861249
scholarrs55861249
googlers55861249
pharmgkbrs55861249
gwascentralrs55861249
openSNPrs55861249
23andMers55861249
23andMe allrs55861249
SNP Nexus

SNPshotrs55861249
SNPdbers55861249
MSV3drs55861249
GWAS Ctlgrs55861249
Max Magnitude0
OMIM607585
Desc
Variant0008
Relatedalso
ClinVar
Risk rs55861249(A,T;A,T)
Alt rs55861249(A,T;A,T)
Reference rs55861249(C;C)
Significance Other
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108098533C>A; NC_000011.9:g.108098533C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000162607.1, RCV000227829.1, RCV000003164.5, RCV000130278.3, RCV000236608.1,