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rs1137887

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1137887(A;A)
Make rs1137887(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108256340
GeneATM
is asnp
is mentioned by
dbSNPrs1137887
ebirs1137887
HLIrs1137887
Exacrs1137887
Varsomers1137887
Maprs1137887
PheGenIrs1137887
hapmaprs1137887
1000 genomesrs1137887
hgdprs1137887
ensemblrs1137887
gopubmedrs1137887
geneviewrs1137887
scholarrs1137887
googlers1137887
pharmgkbrs1137887
gwascentralrs1137887
openSNPrs1137887
23andMers1137887
23andMe allrs1137887
SNP Nexus

SNPshotrs1137887
SNPdbers1137887
MSV3drs1137887
GWAS Ctlgrs1137887
Max Magnitude0
ClinVar
Risk rs1137887(A;A)
Alt rs1137887(A;A)
Reference rs1137887(G;G)
Significance Other
Disease Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108127067G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003185.7, RCV000115149.7, RCV000235101.1,