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rs786203931

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786203931(-;-)
Make rs786203931(-;C)
Make rs786203931(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position94471679
GeneMRE11A
is asnp
is mentioned by
dbSNPrs786203931
ebirs786203931
HLIrs786203931
Exacrs786203931
Varsomers786203931
Maprs786203931
PheGenIrs786203931
hapmaprs786203931
1000 genomesrs786203931
hgdprs786203931
ensemblrs786203931
gopubmedrs786203931
geneviewrs786203931
scholarrs786203931
googlers786203931
pharmgkbrs786203931
gwascentralrs786203931
openSNPrs786203931
23andMers786203931
23andMe allrs786203931
SNP Nexus

SNPshotrs786203931
SNPdbers786203931
MSV3drs786203931
GWAS Ctlgrs786203931
Max Magnitude0
ClinVar
Risk rs786203931(C;C)
Alt rs786203931(C;C)
Reference rs786203931(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.94204846dupG
CLNSRC
CLNACC RCV000167449.1,