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rs876660088

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660088(G;T)
Make rs876660088(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108353765
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876660088
ebirs876660088
HLIrs876660088
Exacrs876660088
Varsomers876660088
Maprs876660088
PheGenIrs876660088
hapmaprs876660088
1000 genomesrs876660088
hgdprs876660088
ensemblrs876660088
gopubmedrs876660088
geneviewrs876660088
scholarrs876660088
googlers876660088
pharmgkbrs876660088
gwascentralrs876660088
openSNPrs876660088
23andMers876660088
23andMe allrs876660088
SNP Nexus

SNPshotrs876660088
SNPdbers876660088
MSV3drs876660088
GWAS Ctlgrs876660088
Max Magnitude0
ClinVar
Risk rs876660088(T;T)
Alt rs876660088(T;T)
Reference rs876660088(G;G)
Significance Probable-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.108224492G>T
CLNSRC
CLNACC RCV000213512.1,