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rs1060501650

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501650(A;A)
Make rs1060501650(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108365111
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs1060501650
dbSNP (classic)rs1060501650
ClinGenrs1060501650
ebirs1060501650
HLIrs1060501650
Exacrs1060501650
Gnomadrs1060501650
Varsomers1060501650
LitVarrs1060501650
Maprs1060501650
PheGenIrs1060501650
Biobankrs1060501650
1000 genomesrs1060501650
hgdprs1060501650
ensemblrs1060501650
geneviewrs1060501650
scholarrs1060501650
googlers1060501650
pharmgkbrs1060501650
gwascentralrs1060501650
openSNPrs1060501650
23andMers1060501650
23andMe allrs1060501650
SNPshotrs1060501650
SNPdbers1060501650
MSV3drs1060501650
GWAS Ctlgrs1060501650
Max Magnitude0
ClinVar
Risk rs1060501650(A;A)
Alt rs1060501650(A;A)
Reference Rs1060501650(G;G)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108235838G>A
CLNSRC
CLNACC RCV000472679.1, RCV000493966.1,