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rs876659569

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659569(-;-)
Make rs876659569(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108326100
GeneATM
is asnp
is mentioned by
dbSNPrs876659569
ebirs876659569
HLIrs876659569
Exacrs876659569
Varsomers876659569
Maprs876659569
PheGenIrs876659569
hapmaprs876659569
1000 genomesrs876659569
hgdprs876659569
ensemblrs876659569
gopubmedrs876659569
geneviewrs876659569
scholarrs876659569
googlers876659569
pharmgkbrs876659569
gwascentralrs876659569
openSNPrs876659569
23andMers876659569
23andMe allrs876659569
SNP Nexus

SNPshotrs876659569
SNPdbers876659569
MSV3drs876659569
GWAS Ctlgrs876659569
Max Magnitude0
ClinVar
Risk rs876659569(;)
Alt rs876659569(;)
Reference rs876659569(G;G)
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.108196827delG
CLNSRC
CLNACC RCV000213820.1,