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rs587779818

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779818(A;A)
Make rs587779818(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108227873
GeneATM
is asnp
is mentioned by
dbSNPrs587779818
ebirs587779818
HLIrs587779818
Exacrs587779818
Varsomers587779818
Maprs587779818
PheGenIrs587779818
hapmaprs587779818
1000 genomesrs587779818
hgdprs587779818
ensemblrs587779818
gopubmedrs587779818
geneviewrs587779818
scholarrs587779818
googlers587779818
pharmgkbrs587779818
gwascentralrs587779818
openSNPrs587779818
23andMers587779818
23andMe allrs587779818
SNP Nexus

SNPshotrs587779818
SNPdbers587779818
MSV3drs587779818
GWAS Ctlgrs587779818
Max Magnitude0
ClinVar
Risk rs587779818(A;A)
Alt rs587779818(A;A)
Reference rs587779818(G;G)
Significance Pathogenic
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.108098600G>A
CLNSRC Inc.
CLNACC RCV000115145.6, RCV000197540.2, RCV000211942.1,