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rs786203682

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786203682(-;-)
Make rs786203682(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position94459572
GeneMRE11A
is asnp
is mentioned by
dbSNPrs786203682
ebirs786203682
HLIrs786203682
Exacrs786203682
Varsomers786203682
Maprs786203682
PheGenIrs786203682
hapmaprs786203682
1000 genomesrs786203682
hgdprs786203682
ensemblrs786203682
gopubmedrs786203682
geneviewrs786203682
scholarrs786203682
googlers786203682
pharmgkbrs786203682
gwascentralrs786203682
openSNPrs786203682
23andMers786203682
23andMe allrs786203682
SNP Nexus

SNPshotrs786203682
SNPdbers786203682
MSV3drs786203682
GWAS Ctlgrs786203682
Max Magnitude0
ClinVar
Risk rs786203682(;)
Alt rs786203682(;)
Reference rs786203682(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.94192738delG
CLNSRC
CLNACC RCV000167093.1,