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rs773516672

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs773516672(A;A)
Make rs773516672(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108330355
GeneATM
is asnp
is mentioned by
dbSNPrs773516672
ebirs773516672
HLIrs773516672
Exacrs773516672
Varsomers773516672
Maprs773516672
PheGenIrs773516672
hapmaprs773516672
1000 genomesrs773516672
hgdprs773516672
ensemblrs773516672
gopubmedrs773516672
geneviewrs773516672
scholarrs773516672
googlers773516672
pharmgkbrs773516672
gwascentralrs773516672
openSNPrs773516672
23andMers773516672
23andMe allrs773516672
SNP Nexus

SNPshotrs773516672
SNPdbers773516672
MSV3drs773516672
GWAS Ctlgrs773516672
Max Magnitude0
ClinVar
Risk rs773516672(A;A)
Alt rs773516672(A;A)
Reference rs773516672(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene C11orf65 ATM
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.108201082G>A
CLNSRC
CLNACC RCV000236176.1,