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rs746623393

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs746623393(A;G)
Make rs746623393(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108312409
GeneATM
is asnp
is mentioned by
dbSNPrs746623393
ebirs746623393
HLIrs746623393
Exacrs746623393
Varsomers746623393
Maprs746623393
PheGenIrs746623393
hapmaprs746623393
1000 genomesrs746623393
hgdprs746623393
ensemblrs746623393
gopubmedrs746623393
geneviewrs746623393
scholarrs746623393
googlers746623393
pharmgkbrs746623393
gwascentralrs746623393
openSNPrs746623393
23andMers746623393
23andMe allrs746623393
SNP Nexus

SNPshotrs746623393
SNPdbers746623393
MSV3drs746623393
GWAS Ctlgrs746623393
Max Magnitude0
ClinVar
Risk rs746623393(G;G)
Alt rs746623393(G;G)
Reference rs746623393(A;A)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene C11orf65 ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108183136A>G
CLNSRC
CLNACC RCV000216360.1,