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rs745677716

From SNPedia

Orientationplus
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
ebirs745677716
HLIrs745677716
Exacrs745677716
Varsomers745677716
Maprs745677716
PheGenIrs745677716
hapmaprs745677716
1000 genomesrs745677716
hgdprs745677716
ensemblrs745677716
gopubmedrs745677716
geneviewrs745677716
scholarrs745677716
googlers745677716
pharmgkbrs745677716
gwascentralrs745677716
openSNPrs745677716
23andMers745677716
23andMe allrs745677716
SNP Nexus

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 RCV000166874.1,