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rs372000848

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs372000848(A;A)
Make rs372000848(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position94470575
GeneMRE11
is asnp
is mentioned by
dbSNPrs372000848
ebirs372000848
HLIrs372000848
Exacrs372000848
Varsomers372000848
Maprs372000848
PheGenIrs372000848
hapmaprs372000848
1000 genomesrs372000848
hgdprs372000848
ensemblrs372000848
gopubmedrs372000848
geneviewrs372000848
scholarrs372000848
googlers372000848
pharmgkbrs372000848
gwascentralrs372000848
openSNPrs372000848
23andMers372000848
23andMe allrs372000848
SNP Nexus

SNPshotrs372000848
SNPdbers372000848
MSV3drs372000848
GWAS Ctlgrs372000848
Max Magnitude0
ClinVar
Risk rs372000848(A;A)
Alt rs372000848(A;A)
Reference rs372000848(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.94203741G>A
CLNSRC
CLNACC RCV000115925.8, RCV000212563.1,