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rs876658572

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876658572(-;-)
Make rs876658572(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108251889
GeneATM
is asnp
is mentioned by
dbSNPrs876658572
ebirs876658572
HLIrs876658572
Exacrs876658572
Varsomers876658572
Maprs876658572
PheGenIrs876658572
hapmaprs876658572
1000 genomesrs876658572
hgdprs876658572
ensemblrs876658572
gopubmedrs876658572
geneviewrs876658572
scholarrs876658572
googlers876658572
pharmgkbrs876658572
gwascentralrs876658572
openSNPrs876658572
23andMers876658572
23andMe allrs876658572
SNP Nexus

SNPshotrs876658572
SNPdbers876658572
MSV3drs876658572
GWAS Ctlgrs876658572
Max Magnitude0
ClinVar
Risk rs876658572(;)
Alt rs876658572(;)
Reference rs876658572(A;A)
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.108122616delA
CLNSRC
CLNACC RCV000221324.1,