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rs730881346

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730881346(G;G)
Make rs730881346(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108257471
GeneATM
is asnp
is mentioned by
dbSNPrs730881346
ebirs730881346
HLIrs730881346
Exacrs730881346
Varsomers730881346
Maprs730881346
PheGenIrs730881346
hapmaprs730881346
1000 genomesrs730881346
hgdprs730881346
ensemblrs730881346
gopubmedrs730881346
geneviewrs730881346
scholarrs730881346
googlers730881346
pharmgkbrs730881346
gwascentralrs730881346
openSNPrs730881346
23andMers730881346
23andMe allrs730881346
SNP Nexus

SNPshotrs730881346
SNPdbers730881346
MSV3drs730881346
GWAS Ctlgrs730881346
Max Magnitude0
ClinVar
Risk rs730881346(G;G)
Alt rs730881346(G;G)
Reference rs730881346(T;T)
Significance Pathogenic
Disease not provided Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN not provided Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108128198T>G
CLNSRC
CLNACC RCV000159691.2, RCV000161929.3,