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rs866402530

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs866402530(A;A)
Make rs866402530(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108335911
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs866402530
ebirs866402530
HLIrs866402530
Exacrs866402530
Varsomers866402530
Maprs866402530
PheGenIrs866402530
hapmaprs866402530
1000 genomesrs866402530
hgdprs866402530
ensemblrs866402530
gopubmedrs866402530
geneviewrs866402530
scholarrs866402530
googlers866402530
pharmgkbrs866402530
gwascentralrs866402530
openSNPrs866402530
23andMers866402530
23andMe allrs866402530
SNP Nexus

SNPshotrs866402530
SNPdbers866402530
MSV3drs866402530
GWAS Ctlgrs866402530
Max Magnitude0
ClinVar
Risk rs866402530(A;A)
Alt rs866402530(A;A)
Reference rs866402530(C;C)
Significance 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.108206638C>T
CLNSRC
CLNACC RCV000220128.1,