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rs876659003

From SNPedia

Orientationplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs876659003(-;-)
Make rs876659003(-;TG)
Make rs876659003(TG;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108244881
GeneATM
is asnp
is mentioned by
dbSNPrs876659003
ebirs876659003
HLIrs876659003
Exacrs876659003
Varsomers876659003
Maprs876659003
PheGenIrs876659003
hapmaprs876659003
1000 genomesrs876659003
hgdprs876659003
ensemblrs876659003
gopubmedrs876659003
geneviewrs876659003
scholarrs876659003
googlers876659003
pharmgkbrs876659003
gwascentralrs876659003
openSNPrs876659003
23andMers876659003
23andMe allrs876659003
SNP Nexus

SNPshotrs876659003
SNPdbers876659003
MSV3drs876659003
GWAS Ctlgrs876659003
Max Magnitude0
ClinVar
Risk rs876659003(;)
Alt rs876659003(;)
Reference rs876659003(GT;GT)
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.108115608_108115609delTG
CLNSRC
CLNACC RCV000222737.1,