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

rs876658548

From SNPedia

Orientationplus
Geno Mag Summary
(GACT;GACT) 0 common in clinvar
Make rs876658548(-;-)
Make rs876658548(-;TGAC)
Make rs876658548(TGAC;TGAC)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108244062
GeneATM
is asnp
is mentioned by
dbSNPrs876658548
ebirs876658548
HLIrs876658548
Exacrs876658548
Varsomers876658548
Maprs876658548
PheGenIrs876658548
hapmaprs876658548
1000 genomesrs876658548
hgdprs876658548
ensemblrs876658548
gopubmedrs876658548
geneviewrs876658548
scholarrs876658548
googlers876658548
pharmgkbrs876658548
gwascentralrs876658548
openSNPrs876658548
23andMers876658548
23andMe allrs876658548
SNP Nexus

SNPshotrs876658548
SNPdbers876658548
MSV3drs876658548
GWAS Ctlgrs876658548
Max Magnitude0
ClinVar
Risk rs876658548(;)
Alt rs876658548(;)
Reference rs876658548(GACT;GACT)
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.108114789_108114792delTGAC
CLNSRC
CLNACC RCV000219082.1,