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rs747832587

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs747832587(-;-)
Make rs747832587(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position94459467
GeneMRE11A
is asnp
is mentioned by
dbSNPrs747832587
dbSNP (old)rs747832587
ClinGenrs747832587
ebirs747832587
HLIrs747832587
Exacrs747832587
Varsomers747832587
Maprs747832587
PheGenIrs747832587
Biobankrs747832587
1000 genomesrs747832587
hgdprs747832587
ensemblrs747832587
gopubmedrs747832587
geneviewrs747832587
scholarrs747832587
googlers747832587
pharmgkbrs747832587
gwascentralrs747832587
openSNPrs747832587
23andMers747832587
23andMe allrs747832587
SNP Nexus

SNPshotrs747832587
SNPdbers747832587
MSV3drs747832587
GWAS Ctlgrs747832587
Max Magnitude0
ClinVar
Risk rs747832587(-;-)
Alt rs747832587(-;-)
Reference Rs747832587(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.94192633delT
CLNSRC
CLNACC RCV000199221.1,