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rs786202032

From SNPedia

Orientationminus
Geno Mag Summary
(TTT;TTT) 0 common in clinvar
Make rs786202032(A;A)
Make rs786202032(A;TTT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position94471596
GeneMRE11A
is asnp
is mentioned by
dbSNPrs786202032
ebirs786202032
HLIrs786202032
Exacrs786202032
Varsomers786202032
Maprs786202032
PheGenIrs786202032
hapmaprs786202032
1000 genomesrs786202032
hgdprs786202032
ensemblrs786202032
gopubmedrs786202032
geneviewrs786202032
scholarrs786202032
googlers786202032
pharmgkbrs786202032
gwascentralrs786202032
openSNPrs786202032
23andMers786202032
23andMe allrs786202032
SNP Nexus

SNPshotrs786202032
SNPdbers786202032
MSV3drs786202032
GWAS Ctlgrs786202032
Max Magnitude0
ClinVar
Risk rs786202032(A;A)
Alt rs786202032(A;A)
Reference rs786202032(TTT;TTT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.94204762_94204764delAAAinsT
CLNSRC
CLNACC RCV000164635.1,