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rs1057516833

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057516833(C;G)
Make rs1057516833(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108329097
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs1057516833
dbSNP (old)rs1057516833
ClinGenrs1057516833
ebirs1057516833
HLIrs1057516833
Exacrs1057516833
Gnomadrs1057516833
Varsomers1057516833
Maprs1057516833
PheGenIrs1057516833
Biobankrs1057516833
1000 genomesrs1057516833
hgdprs1057516833
ensemblrs1057516833
gopubmedrs1057516833
geneviewrs1057516833
scholarrs1057516833
googlers1057516833
pharmgkbrs1057516833
gwascentralrs1057516833
openSNPrs1057516833
23andMers1057516833
23andMe allrs1057516833
SNPshotrs1057516833
SNPdbers1057516833
MSV3drs1057516833
GWAS Ctlgrs1057516833
Max Magnitude0
ClinVar
Risk rs1057516833(G;G) rs1057516833(T;T)
Alt rs1057516833(G;G) rs1057516833(T;T)
Reference Rs1057516833(C;C)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome not specified
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia syndrome not specified
Reversed 0
HGVS NC_000011.9:g.108199824C>G; NC_000011.9:g.108199824C>T
CLNSRC
CLNACC RCV000411247.1, RCV000436625.1,