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rs201963507

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs201963507(A;G)
Make rs201963507(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108310287
GeneATM
is asnp
is mentioned by
dbSNPrs201963507
ebirs201963507
HLIrs201963507
Exacrs201963507
Varsomers201963507
Maprs201963507
PheGenIrs201963507
hapmaprs201963507
1000 genomesrs201963507
hgdprs201963507
ensemblrs201963507
gopubmedrs201963507
geneviewrs201963507
scholarrs201963507
googlers201963507
pharmgkbrs201963507
gwascentralrs201963507
openSNPrs201963507
23andMers201963507
23andMe allrs201963507
SNP Nexus

SNPshotrs201963507
SNPdbers201963507
MSV3drs201963507
GWAS Ctlgrs201963507
Max Magnitude0
ClinVar
Risk rs201963507(G,T;G,T)
Alt rs201963507(G,T;G,T)
Reference rs201963507(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not specified not provided
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not specified not provided
Reversed 0
HGVS NC_000011.9:g.108181014A>G; NC_000011.9:g.108181014A>T
CLNSRC
CLNACC RCV000130965.4, RCV000197688.2, RCV000212034.2, RCV000159769.2, RCV000206728.1,