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rs876660382

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660382(G;T)
Make rs876660382(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108365356
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876660382
ebirs876660382
HLIrs876660382
Exacrs876660382
Varsomers876660382
Maprs876660382
PheGenIrs876660382
hapmaprs876660382
1000 genomesrs876660382
hgdprs876660382
ensemblrs876660382
gopubmedrs876660382
geneviewrs876660382
scholarrs876660382
googlers876660382
pharmgkbrs876660382
gwascentralrs876660382
openSNPrs876660382
23andMers876660382
23andMe allrs876660382
SNP Nexus

SNPshotrs876660382
SNPdbers876660382
MSV3drs876660382
GWAS Ctlgrs876660382
Max Magnitude0
ClinVar
Risk rs876660382(T;T)
Alt rs876660382(T;T)
Reference rs876660382(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Ataxia-telangiectasia syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108236083G>T
CLNSRC
CLNACC RCV000222768.1, RCV000233073.1,