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rs876659672

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659672(-;-)
Make rs876659672(-;G)
Make rs876659672(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108284415
GeneATM
is asnp
is mentioned by
dbSNPrs876659672
ebirs876659672
HLIrs876659672
Exacrs876659672
Varsomers876659672
Maprs876659672
PheGenIrs876659672
hapmaprs876659672
1000 genomesrs876659672
hgdprs876659672
ensemblrs876659672
gopubmedrs876659672
geneviewrs876659672
scholarrs876659672
googlers876659672
pharmgkbrs876659672
gwascentralrs876659672
openSNPrs876659672
23andMers876659672
23andMe allrs876659672
SNP Nexus

SNPshotrs876659672
SNPdbers876659672
MSV3drs876659672
GWAS Ctlgrs876659672
Max Magnitude0
ClinVar
Risk rs876659672(G;G)
Alt rs876659672(G;G)
Reference rs876659672(;)
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.108155142dupG
CLNSRC
CLNACC RCV000223199.1,