Have questions? Visit https://www.reddit.com/r/SNPedia

rs202206540

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202206540(A;A)
Make rs202206540(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108316069
GeneATM
is asnp
is mentioned by
dbSNPrs202206540
ebirs202206540
HLIrs202206540
Exacrs202206540
Varsomers202206540
Maprs202206540
PheGenIrs202206540
hapmaprs202206540
1000 genomesrs202206540
hgdprs202206540
ensemblrs202206540
gopubmedrs202206540
geneviewrs202206540
scholarrs202206540
googlers202206540
pharmgkbrs202206540
gwascentralrs202206540
openSNPrs202206540
23andMers202206540
23andMe allrs202206540
SNP Nexus

SNPshotrs202206540
SNPdbers202206540
MSV3drs202206540
GWAS Ctlgrs202206540
Max Magnitude0
ClinVar
Risk rs202206540(A;A)
Alt rs202206540(A;A)
Reference rs202206540(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not specified
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not specified
Reversed 0
HGVS NC_000011.9:g.108186796G>A
CLNSRC
CLNACC RCV000159743.4, RCV000167963.2, RCV000212039.1,