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rs876660567

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660567(-;-)
Make rs876660567(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108354826
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876660567
ebirs876660567
HLIrs876660567
Exacrs876660567
Varsomers876660567
Maprs876660567
PheGenIrs876660567
hapmaprs876660567
1000 genomesrs876660567
hgdprs876660567
ensemblrs876660567
gopubmedrs876660567
geneviewrs876660567
scholarrs876660567
googlers876660567
pharmgkbrs876660567
gwascentralrs876660567
openSNPrs876660567
23andMers876660567
23andMe allrs876660567
SNP Nexus

SNPshotrs876660567
SNPdbers876660567
MSV3drs876660567
GWAS Ctlgrs876660567
Max Magnitude0
ClinVar
Risk rs876660567(;)
Alt rs876660567(;)
Reference rs876660567(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene C11orf65 ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108225553delC
CLNSRC
CLNACC RCV000218511.1,