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rs587779813

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779813(A;A)
Make rs587779813(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108249102
GeneATM
is asnp
is mentioned by
dbSNPrs587779813
ebirs587779813
HLIrs587779813
Exacrs587779813
Varsomers587779813
Maprs587779813
PheGenIrs587779813
hapmaprs587779813
1000 genomesrs587779813
hgdprs587779813
ensemblrs587779813
gopubmedrs587779813
geneviewrs587779813
scholarrs587779813
googlers587779813
pharmgkbrs587779813
gwascentralrs587779813
openSNPrs587779813
23andMers587779813
23andMe allrs587779813
SNP Nexus

SNPshotrs587779813
SNPdbers587779813
MSV3drs587779813
GWAS Ctlgrs587779813
Max Magnitude0
ClinVar
Risk rs587779813(A;A)
Alt rs587779813(A;A)
Reference rs587779813(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ATM
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.108119829G>A
CLNSRC
CLNACC RCV000115138.3,