Have questions? Visit https://www.reddit.com/r/SNPedia

rs786202764

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786202764(-;-)
Make rs786202764(-;C)
Make rs786202764(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position94464202
GeneMRE11A
is asnp
is mentioned by
dbSNPrs786202764
ebirs786202764
HLIrs786202764
Exacrs786202764
Varsomers786202764
Maprs786202764
PheGenIrs786202764
hapmaprs786202764
1000 genomesrs786202764
hgdprs786202764
ensemblrs786202764
gopubmedrs786202764
geneviewrs786202764
scholarrs786202764
googlers786202764
pharmgkbrs786202764
gwascentralrs786202764
openSNPrs786202764
23andMers786202764
23andMe allrs786202764
SNP Nexus

SNPshotrs786202764
SNPdbers786202764
MSV3drs786202764
GWAS Ctlgrs786202764
Max Magnitude0
ClinVar
Risk rs786202764(C;C)
Alt rs786202764(C;C)
Reference rs786202764(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.94197369dupG
CLNSRC
CLNACC RCV000165739.1,