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rs112805604

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs112805604(A;A)
Make rs112805604(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108227889
GeneATM
is asnp
is mentioned by
dbSNPrs112805604
ebirs112805604
HLIrs112805604
Exacrs112805604
Varsomers112805604
Maprs112805604
PheGenIrs112805604
hapmaprs112805604
1000 genomesrs112805604
hgdprs112805604
ensemblrs112805604
gopubmedrs112805604
geneviewrs112805604
scholarrs112805604
googlers112805604
pharmgkbrs112805604
gwascentralrs112805604
openSNPrs112805604
23andMers112805604
23andMe allrs112805604
SNP Nexus

SNPshotrs112805604
SNPdbers112805604
MSV3drs112805604
GWAS Ctlgrs112805604
Max Magnitude0
ClinVar
Risk rs112805604(A;A)
Alt rs112805604(A;A)
Reference rs112805604(G;G)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108098616G>A
CLNSRC
CLNACC RCV000205116.2,