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rs768362387

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768362387(A;A)
Make rs768362387(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108253846
GeneATM
is asnp
is mentioned by
dbSNPrs768362387
ebirs768362387
HLIrs768362387
Exacrs768362387
Varsomers768362387
Maprs768362387
PheGenIrs768362387
hapmaprs768362387
1000 genomesrs768362387
hgdprs768362387
ensemblrs768362387
gopubmedrs768362387
geneviewrs768362387
scholarrs768362387
googlers768362387
pharmgkbrs768362387
gwascentralrs768362387
openSNPrs768362387
23andMers768362387
23andMe allrs768362387
SNP Nexus

SNPshotrs768362387
SNPdbers768362387
MSV3drs768362387
GWAS Ctlgrs768362387
Max Magnitude0
ClinVar
Risk rs768362387(A;A)
Alt rs768362387(A;A)
Reference rs768362387(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.108124573C>A
CLNSRC
CLNACC RCV000222313.1,