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rs876658959

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658959(-;-)
Make rs876658959(-;AACT)
Make rs876658959(AACT;AACT)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108354845
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876658959
ebirs876658959
HLIrs876658959
Exacrs876658959
Varsomers876658959
Maprs876658959
PheGenIrs876658959
hapmaprs876658959
1000 genomesrs876658959
hgdprs876658959
ensemblrs876658959
gopubmedrs876658959
geneviewrs876658959
scholarrs876658959
googlers876658959
pharmgkbrs876658959
gwascentralrs876658959
openSNPrs876658959
23andMers876658959
23andMe allrs876658959
SNP Nexus

SNPshotrs876658959
SNPdbers876658959
MSV3drs876658959
GWAS Ctlgrs876658959
Max Magnitude0
ClinVar
Risk rs876658959(AACT;AACT)
Alt rs876658959(AACT;AACT)
Reference rs876658959(;)
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.108225569_108225572dupAACT
CLNSRC
CLNACC RCV000217008.1,