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

rs746235533

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs746235533(C;T)
Make rs746235533(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108227691
GeneATM
is asnp
is mentioned by
dbSNPrs746235533
ebirs746235533
HLIrs746235533
Exacrs746235533
Varsomers746235533
Maprs746235533
PheGenIrs746235533
hapmaprs746235533
1000 genomesrs746235533
hgdprs746235533
ensemblrs746235533
gopubmedrs746235533
geneviewrs746235533
scholarrs746235533
googlers746235533
pharmgkbrs746235533
gwascentralrs746235533
openSNPrs746235533
23andMers746235533
23andMe allrs746235533
SNP Nexus

SNPshotrs746235533
SNPdbers746235533
MSV3drs746235533
GWAS Ctlgrs746235533
Max Magnitude0
ClinVar
Risk rs746235533(T;T)
Alt rs746235533(T;T)
Reference rs746235533(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108098418C>T
CLNSRC
CLNACC RCV000215307.1,