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

rs750663117

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs750663117(A;A)
Make rs750663117(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108272531
GeneATM
is asnp
is mentioned by
dbSNPrs750663117
dbSNP (old)rs750663117
ClinGenrs750663117
ebirs750663117
HLIrs750663117
Exacrs750663117
Gnomadrs750663117
Varsomers750663117
Maprs750663117
PheGenIrs750663117
Biobankrs750663117
1000 genomesrs750663117
hgdprs750663117
ensemblrs750663117
gopubmedrs750663117
geneviewrs750663117
scholarrs750663117
googlers750663117
pharmgkbrs750663117
gwascentralrs750663117
openSNPrs750663117
23andMers750663117
23andMe allrs750663117
SNP Nexus

SNPshotrs750663117
SNPdbers750663117
MSV3drs750663117
GWAS Ctlgrs750663117
Max Magnitude0
ClinVar
Risk rs750663117(A;A)
Alt rs750663117(A;A)
Reference Rs750663117(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108143258G>A
CLNSRC
CLNACC RCV000219914.2, RCV000410565.1, RCV000482905.1,