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rs876660245

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660245(A;A)
Make rs876660245(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108304674
GeneATM
is asnp
is mentioned by
dbSNPrs876660245
ebirs876660245
HLIrs876660245
Exacrs876660245
Varsomers876660245
Maprs876660245
PheGenIrs876660245
hapmaprs876660245
1000 genomesrs876660245
hgdprs876660245
ensemblrs876660245
gopubmedrs876660245
geneviewrs876660245
scholarrs876660245
googlers876660245
pharmgkbrs876660245
gwascentralrs876660245
openSNPrs876660245
23andMers876660245
23andMe allrs876660245
SNP Nexus

SNPshotrs876660245
SNPdbers876660245
MSV3drs876660245
GWAS Ctlgrs876660245
Max Magnitude0
ClinVar
Risk rs876660245(A;A)
Alt rs876660245(A;A)
Reference rs876660245(G;G)
Significance Probable-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.108175401G>A
CLNSRC
CLNACC RCV000220437.1,