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rs776912688

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs776912688(A;A)
Make rs776912688(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position94471613
GeneMRE11, MRE11A
is asnp
is mentioned by
dbSNPrs776912688
dbSNP (classic)rs776912688
ClinGenrs776912688
ebirs776912688
HLIrs776912688
Exacrs776912688
Gnomadrs776912688
Varsomers776912688
LitVarrs776912688
Maprs776912688
PheGenIrs776912688
Biobankrs776912688
1000 genomesrs776912688
hgdprs776912688
ensemblrs776912688
geneviewrs776912688
scholarrs776912688
googlers776912688
pharmgkbrs776912688
gwascentralrs776912688
openSNPrs776912688
23andMers776912688
SNPshotrs776912688
SNPdbers776912688
MSV3drs776912688
GWAS Ctlgrs776912688
Max Magnitude0
ClinVar
Risk rs776912688(A;A) rs776912688(C;C)
Alt rs776912688(A;A) rs776912688(C;C)
Reference Rs776912688(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11 MRE11A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.94204779G>C
CLNSRC
CLNACC RCV000219565.1,