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rs201089102

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201089102(G;T)
Make rs201089102(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108247128
GeneATM
is asnp
is mentioned by
dbSNPrs201089102
ebirs201089102
HLIrs201089102
Exacrs201089102
Varsomers201089102
Maprs201089102
PheGenIrs201089102
hapmaprs201089102
1000 genomesrs201089102
hgdprs201089102
ensemblrs201089102
gopubmedrs201089102
geneviewrs201089102
scholarrs201089102
googlers201089102
pharmgkbrs201089102
gwascentralrs201089102
openSNPrs201089102
23andMers201089102
23andMe allrs201089102
SNP Nexus

SNPshotrs201089102
SNPdbers201089102
MSV3drs201089102
GWAS Ctlgrs201089102
Max Magnitude0
ClinVar
Risk rs201089102(T;T)
Alt rs201089102(T;T)
Reference rs201089102(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108117855G>T
CLNSRC
CLNACC RCV000166070.1,