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rs730881752

From SNPedia

Orientationminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs730881752(-;-)
Make rs730881752(-;TT)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position94476320
GeneMRE11A
is asnp
is mentioned by
dbSNPrs730881752
ebirs730881752
HLIrs730881752
Exacrs730881752
Varsomers730881752
Maprs730881752
PheGenIrs730881752
hapmaprs730881752
1000 genomesrs730881752
hgdprs730881752
ensemblrs730881752
gopubmedrs730881752
geneviewrs730881752
scholarrs730881752
googlers730881752
pharmgkbrs730881752
gwascentralrs730881752
openSNPrs730881752
23andMers730881752
23andMe allrs730881752
SNP Nexus

SNPshotrs730881752
SNPdbers730881752
MSV3drs730881752
GWAS Ctlgrs730881752
Max Magnitude0
ClinVar
Risk rs730881752(;)
Alt rs730881752(;)
Reference rs730881752(TT;TT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.94209486_94209487delAA
CLNSRC
CLNACC RCV000160577.1,