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rs1057517097

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517097(-;T)
Make rs1057517097(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108272799
GeneATM
is asnp
is mentioned by
dbSNPrs1057517097
dbSNP (old)rs1057517097
ClinGenrs1057517097
ebirs1057517097
HLIrs1057517097
Exacrs1057517097
Gnomadrs1057517097
Varsomers1057517097
Maprs1057517097
PheGenIrs1057517097
Biobankrs1057517097
1000 genomesrs1057517097
hgdprs1057517097
ensemblrs1057517097
gopubmedrs1057517097
geneviewrs1057517097
scholarrs1057517097
googlers1057517097
pharmgkbrs1057517097
gwascentralrs1057517097
openSNPrs1057517097
23andMers1057517097
23andMe allrs1057517097
SNPshotrs1057517097
SNPdbers1057517097
MSV3drs1057517097
GWAS Ctlgrs1057517097
Max Magnitude0
ClinVar
Risk rs1057517097(T;T)
Alt rs1057517097(T;T)
Reference Rs1057517097(-;-)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108143526dupT
CLNSRC
CLNACC RCV000409693.1,