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rs876659866

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs876659866(-;-)
Make rs876659866(-;GT)
Make rs876659866(GT;GT)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108250859
GeneATM
is asnp
is mentioned by
dbSNPrs876659866
ebirs876659866
HLIrs876659866
Exacrs876659866
Varsomers876659866
Maprs876659866
PheGenIrs876659866
hapmaprs876659866
1000 genomesrs876659866
hgdprs876659866
ensemblrs876659866
gopubmedrs876659866
geneviewrs876659866
scholarrs876659866
googlers876659866
pharmgkbrs876659866
gwascentralrs876659866
openSNPrs876659866
23andMers876659866
23andMe allrs876659866
SNP Nexus

SNPshotrs876659866
SNPdbers876659866
MSV3drs876659866
GWAS Ctlgrs876659866
Max Magnitude0
ClinVar
Risk rs876659866(;)
Alt rs876659866(;)
Reference rs876659866(TG;TG)
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.108121586_108121587delGT
CLNSRC
CLNACC RCV000216302.1,