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rs779269083

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs779269083(A;A)
Make rs779269083(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position94486009
GeneMRE11
is asnp
is mentioned by
dbSNPrs779269083
ebirs779269083
HLIrs779269083
Exacrs779269083
Varsomers779269083
Maprs779269083
PheGenIrs779269083
hapmaprs779269083
1000 genomesrs779269083
hgdprs779269083
ensemblrs779269083
gopubmedrs779269083
geneviewrs779269083
scholarrs779269083
googlers779269083
pharmgkbrs779269083
gwascentralrs779269083
openSNPrs779269083
23andMers779269083
23andMe allrs779269083
SNP Nexus

SNPshotrs779269083
SNPdbers779269083
MSV3drs779269083
GWAS Ctlgrs779269083
Max Magnitude0
ClinVar
Risk rs779269083(A,T;A,T)
Alt rs779269083(A,T;A,T)
Reference rs779269083(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.94219175C>A
CLNSRC
CLNACC RCV000210166.1, RCV000221654.1,