Have questions? Visit https://www.reddit.com/r/SNPedia

rs876658502

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658502(-;-)
Make rs876658502(-;A)
Make rs876658502(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108272539
GeneATM
is asnp
is mentioned by
dbSNPrs876658502
ebirs876658502
HLIrs876658502
Exacrs876658502
Varsomers876658502
Maprs876658502
PheGenIrs876658502
hapmaprs876658502
1000 genomesrs876658502
hgdprs876658502
ensemblrs876658502
gopubmedrs876658502
geneviewrs876658502
scholarrs876658502
googlers876658502
pharmgkbrs876658502
gwascentralrs876658502
openSNPrs876658502
23andMers876658502
23andMe allrs876658502
SNP Nexus

SNPshotrs876658502
SNPdbers876658502
MSV3drs876658502
GWAS Ctlgrs876658502
Max Magnitude0
ClinVar
Risk rs876658502(A;A)
Alt rs876658502(A;A)
Reference rs876658502(;)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 0
HGVS NC_000011.9:g.108143266dupA
CLNSRC
CLNACC RCV000220687.1, RCV000236766.1,