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rs876659535

From SNPedia

Orientationplus
Geno Mag Summary
(GATA;GATA) 0 common in clinvar
Make rs876659535(-;-)
Make rs876659535(-;GATA)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108293343
GeneATM
is asnp
is mentioned by
dbSNPrs876659535
ebirs876659535
HLIrs876659535
Exacrs876659535
Varsomers876659535
Maprs876659535
PheGenIrs876659535
hapmaprs876659535
1000 genomesrs876659535
hgdprs876659535
ensemblrs876659535
gopubmedrs876659535
geneviewrs876659535
scholarrs876659535
googlers876659535
pharmgkbrs876659535
gwascentralrs876659535
openSNPrs876659535
23andMers876659535
23andMe allrs876659535
SNP Nexus

SNPshotrs876659535
SNPdbers876659535
MSV3drs876659535
GWAS Ctlgrs876659535
Max Magnitude0
ClinVar
Risk rs876659535(;)
Alt rs876659535(;)
Reference rs876659535(GATA;GATA)
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.108164070_108164073delGATA
CLNSRC
CLNACC RCV000214019.1,