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rs876658402

From SNPedia

Orientationplus
Geno Mag Summary
(CAAGTTCG;CAAGTTCG) 0 common in clinvar
Make rs876658402(-;-)
Make rs876658402(-;AGTTCGCA)
Make rs876658402(AGTTCGCA;AGTTCGCA)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108272820
GeneATM
is asnp
is mentioned by
dbSNPrs876658402
ebirs876658402
HLIrs876658402
Exacrs876658402
Varsomers876658402
Maprs876658402
PheGenIrs876658402
hapmaprs876658402
1000 genomesrs876658402
hgdprs876658402
ensemblrs876658402
gopubmedrs876658402
geneviewrs876658402
scholarrs876658402
googlers876658402
pharmgkbrs876658402
gwascentralrs876658402
openSNPrs876658402
23andMers876658402
23andMe allrs876658402
SNP Nexus

SNPshotrs876658402
SNPdbers876658402
MSV3drs876658402
GWAS Ctlgrs876658402
Max Magnitude0
ClinVar
Risk rs876658402(;)
Alt rs876658402(;)
Reference rs876658402(CAAGTTCG;CAAGTTCG)
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.108143547_108143554delAGTTCGCA
CLNSRC
CLNACC RCV000215432.1,