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rs876660783

From SNPedia

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Geno Mag Summary
(TAGAA;TAGAA) 0 common in clinvar
Make rs876660783(G;G)
Make rs876660783(G;TAGAA)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108282750
GeneATM
is asnp
is mentioned by
dbSNPrs876660783
ebirs876660783
HLIrs876660783
Exacrs876660783
Varsomers876660783
Maprs876660783
PheGenIrs876660783
hapmaprs876660783
1000 genomesrs876660783
hgdprs876660783
ensemblrs876660783
gopubmedrs876660783
geneviewrs876660783
scholarrs876660783
googlers876660783
pharmgkbrs876660783
gwascentralrs876660783
openSNPrs876660783
23andMers876660783
23andMe allrs876660783
SNP Nexus

SNPshotrs876660783
SNPdbers876660783
MSV3drs876660783
GWAS Ctlgrs876660783
Max Magnitude0
ClinVar
Risk rs876660783(G;G)
Alt rs876660783(G;G)
Reference rs876660783(TAGAA;TAGAA)
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.108153477_108153481delTAGAAinsG
CLNSRC
CLNACC RCV000215411.1,