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rs863224462

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224462(C;T)
Make rs863224462(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108329171
GeneATM
is asnp
is mentioned by
dbSNPrs863224462
ebirs863224462
HLIrs863224462
Exacrs863224462
Varsomers863224462
Maprs863224462
PheGenIrs863224462
hapmaprs863224462
1000 genomesrs863224462
hgdprs863224462
ensemblrs863224462
gopubmedrs863224462
geneviewrs863224462
scholarrs863224462
googlers863224462
pharmgkbrs863224462
gwascentralrs863224462
openSNPrs863224462
23andMers863224462
23andMe allrs863224462
SNP Nexus

SNPshotrs863224462
SNPdbers863224462
MSV3drs863224462
GWAS Ctlgrs863224462
Max Magnitude0
ClinVar
Risk rs863224462(T;T)
Alt rs863224462(T;T)
Reference rs863224462(C;C)
Significance Pathogenic
Disease not specified Ataxia-telangiectasia syndrome
Variation info
Gene C11orf65 ATM
CLNDBN not specified Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108199898C>A; NC_000011.9:g.108199898C>T
CLNSRC
CLNACC RCV000236245.1, RCV000200187.2,