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rs745677716

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs745677716(A;G)
Make rs745677716(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position94445808
GeneMRE11A
is asnp
is mentioned by
dbSNPrs745677716
dbSNP (classic)rs745677716
ClinGenrs745677716
ebirs745677716
HLIrs745677716
Exacrs745677716
Gnomadrs745677716
Varsomers745677716
LitVarrs745677716
Maprs745677716
PheGenIrs745677716
Biobankrs745677716
1000 genomesrs745677716
hgdprs745677716
ensemblrs745677716
geneviewrs745677716
scholarrs745677716
googlers745677716
pharmgkbrs745677716
gwascentralrs745677716
openSNPrs745677716
23andMers745677716
SNPshotrs745677716
SNPdbers745677716
MSV3drs745677716
GWAS Ctlgrs745677716
Max Magnitude0
ClinVar
Risk rs745677716(G;G)
Alt rs745677716(G;G)
Reference Rs745677716(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.94178974A>G
CLNSRC
CLNACC RCV000166874.2,