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rs786203314

From SNPedia

Orientationminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs786203314(AG;TTAA)
Make rs786203314(TTAA;TTAA)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position94459462
GeneMRE11A
is asnp
is mentioned by
dbSNPrs786203314
ebirs786203314
HLIrs786203314
Exacrs786203314
Varsomers786203314
Maprs786203314
PheGenIrs786203314
hapmaprs786203314
1000 genomesrs786203314
hgdprs786203314
ensemblrs786203314
gopubmedrs786203314
geneviewrs786203314
scholarrs786203314
googlers786203314
pharmgkbrs786203314
gwascentralrs786203314
openSNPrs786203314
23andMers786203314
23andMe allrs786203314
SNP Nexus

SNPshotrs786203314
SNPdbers786203314
MSV3drs786203314
GWAS Ctlgrs786203314
Max Magnitude0
ClinVar
Risk rs786203314(TTAA;TTAA)
Alt rs786203314(TTAA;TTAA)
Reference rs786203314(AG;AG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.94192628_94192629delCTinsTTAA
CLNSRC
CLNACC RCV000166568.1,