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rs587779822

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779822(-;-)
Make rs587779822(-;A)
Make rs587779822(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108267206
GeneATM
is asnp
is mentioned by
dbSNPrs587779822
ebirs587779822
HLIrs587779822
Exacrs587779822
Varsomers587779822
Maprs587779822
PheGenIrs587779822
hapmaprs587779822
1000 genomesrs587779822
hgdprs587779822
ensemblrs587779822
gopubmedrs587779822
geneviewrs587779822
scholarrs587779822
googlers587779822
pharmgkbrs587779822
gwascentralrs587779822
openSNPrs587779822
23andMers587779822
23andMe allrs587779822
SNP Nexus

SNPshotrs587779822
SNPdbers587779822
MSV3drs587779822
GWAS Ctlgrs587779822
Max Magnitude0
ClinVar
Risk rs587779822(A;A)
Alt rs587779822(A;A)
Reference rs587779822(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108137933dupA
CLNSRC
CLNACC RCV000115156.5, RCV000235098.1,