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rs876658512

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876658512(-;-)
Make rs876658512(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108327757
GeneATM
is asnp
is mentioned by
dbSNPrs876658512
ebirs876658512
HLIrs876658512
Exacrs876658512
Varsomers876658512
Maprs876658512
PheGenIrs876658512
hapmaprs876658512
1000 genomesrs876658512
hgdprs876658512
ensemblrs876658512
gopubmedrs876658512
geneviewrs876658512
scholarrs876658512
googlers876658512
pharmgkbrs876658512
gwascentralrs876658512
openSNPrs876658512
23andMers876658512
23andMe allrs876658512
SNP Nexus

SNPshotrs876658512
SNPdbers876658512
MSV3drs876658512
GWAS Ctlgrs876658512
Max Magnitude0
ClinVar
Risk rs876658512(;)
Alt rs876658512(;)
Reference rs876658512(A;A)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Ataxia-telangiectasia syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108198484delA
CLNSRC
CLNACC RCV000216898.1, RCV000223734.1,