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rs876658917

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658917(A;A)
Make rs876658917(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position94471760
GeneMRE11
is asnp
is mentioned by
dbSNPrs876658917
ClinGenrs876658917
ebirs876658917
HLIrs876658917
Exacrs876658917
Varsomers876658917
Maprs876658917
PheGenIrs876658917
hapmaprs876658917
1000 genomesrs876658917
hgdprs876658917
ensemblrs876658917
gopubmedrs876658917
geneviewrs876658917
scholarrs876658917
googlers876658917
pharmgkbrs876658917
gwascentralrs876658917
openSNPrs876658917
23andMers876658917
23andMe allrs876658917
SNP Nexus

SNPshotrs876658917
SNPdbers876658917
MSV3drs876658917
GWAS Ctlgrs876658917
Max Magnitude0
ClinVar
Risk rs876658917(A;A)
Alt rs876658917(A;A)
Reference Rs876658917(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.94204926C>T
CLNSRC
CLNACC RCV000220497.1,