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rs876660430

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660430(G;T)
Make rs876660430(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108267204
GeneATM
is asnp
is mentioned by
dbSNPrs876660430
ebirs876660430
HLIrs876660430
Exacrs876660430
Varsomers876660430
Maprs876660430
PheGenIrs876660430
hapmaprs876660430
1000 genomesrs876660430
hgdprs876660430
ensemblrs876660430
gopubmedrs876660430
geneviewrs876660430
scholarrs876660430
googlers876660430
pharmgkbrs876660430
gwascentralrs876660430
openSNPrs876660430
23andMers876660430
23andMe allrs876660430
SNP Nexus

SNPshotrs876660430
SNPdbers876660430
MSV3drs876660430
GWAS Ctlgrs876660430
Max Magnitude0
ClinVar
Risk rs876660430(T;T)
Alt rs876660430(T;T)
Reference rs876660430(G;G)
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.108137931G>T
CLNSRC
CLNACC RCV000218880.1,