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rs786203606

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786203606(C;C)
Make rs786203606(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108227626
GeneATM
is asnp
is mentioned by
dbSNPrs786203606
ebirs786203606
HLIrs786203606
Exacrs786203606
Varsomers786203606
Maprs786203606
PheGenIrs786203606
hapmaprs786203606
1000 genomesrs786203606
hgdprs786203606
ensemblrs786203606
gopubmedrs786203606
geneviewrs786203606
scholarrs786203606
googlers786203606
pharmgkbrs786203606
gwascentralrs786203606
openSNPrs786203606
23andMers786203606
23andMe allrs786203606
SNP Nexus

SNPshotrs786203606
SNPdbers786203606
MSV3drs786203606
GWAS Ctlgrs786203606
Max Magnitude0
ClinVar
Risk rs786203606(C;C)
Alt rs786203606(C;C)
Reference rs786203606(T;T)
Significance Other
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108098353T>C
CLNSRC
CLNACC RCV000166992.1, RCV000168377.5,