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rs1060501700

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060501700(A;C)
Make rs1060501700(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108347277
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs1060501700
dbSNP (old)rs1060501700
ClinGenrs1060501700
ebirs1060501700
HLIrs1060501700
Exacrs1060501700
Gnomadrs1060501700
Varsomers1060501700
Maprs1060501700
PheGenIrs1060501700
Biobankrs1060501700
1000 genomesrs1060501700
hgdprs1060501700
ensemblrs1060501700
gopubmedrs1060501700
geneviewrs1060501700
scholarrs1060501700
googlers1060501700
pharmgkbrs1060501700
gwascentralrs1060501700
openSNPrs1060501700
23andMers1060501700
23andMe allrs1060501700
SNPshotrs1060501700
SNPdbers1060501700
MSV3drs1060501700
GWAS Ctlgrs1060501700
Max Magnitude0
ClinVar
Risk rs1060501700(C;C)
Alt rs1060501700(C;C)
Reference Rs1060501700(A;A)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108218004A>C
CLNSRC
CLNACC RCV000462876.1, RCV000482474.1,