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rs876659116

From SNPedia

Orientationplus
Geno Mag Summary
(AATT;AATT) 0 common in clinvar
Make rs876659116(-;-)
Make rs876659116(-;TTAA)
Make rs876659116(TTAA;TTAA)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108227822
GeneATM
is asnp
is mentioned by
dbSNPrs876659116
ebirs876659116
HLIrs876659116
Exacrs876659116
Varsomers876659116
Maprs876659116
PheGenIrs876659116
hapmaprs876659116
1000 genomesrs876659116
hgdprs876659116
ensemblrs876659116
gopubmedrs876659116
geneviewrs876659116
scholarrs876659116
googlers876659116
pharmgkbrs876659116
gwascentralrs876659116
openSNPrs876659116
23andMers876659116
23andMe allrs876659116
SNP Nexus

SNPshotrs876659116
SNPdbers876659116
MSV3drs876659116
GWAS Ctlgrs876659116
Max Magnitude0
ClinVar
Risk rs876659116(;)
Alt rs876659116(;)
Reference rs876659116(AATT;AATT)
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.108098549_108098552delTTAA
CLNSRC
CLNACC RCV000220926.1,