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rs532480170

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs532480170(A;A)
Make rs532480170(A;C)
ReferenceGRCh38 38.1/142
Chromosome11
Position108316015
GeneATM
is asnp
is mentioned by
dbSNPrs532480170
ebirs532480170
HLIrs532480170
Exacrs532480170
Varsomers532480170
Maprs532480170
PheGenIrs532480170
hapmaprs532480170
1000 genomesrs532480170
hgdprs532480170
ensemblrs532480170
gopubmedrs532480170
geneviewrs532480170
scholarrs532480170
googlers532480170
pharmgkbrs532480170
gwascentralrs532480170
openSNPrs532480170
23andMers532480170
23andMe allrs532480170
SNP Nexus

SNPshotrs532480170
SNPdbers532480170
MSV3drs532480170
GWAS Ctlgrs532480170
Max Magnitude0
ClinVar
Risk rs532480170(A,T;A,T)
Alt rs532480170(A,T;A,T)
Reference rs532480170(C;C)
Significance Other
Disease Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108186742C>A; NC_000011.9:g.108186742C>T
CLNSRC Inc.
CLNACC RCV000215954.1, RCV000115222.6, RCV000122867.3, RCV000235108.1,