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Variant (rsID / SNP)

rs779269083

MRE11

rs779269083 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRE11. Location: chromosome 11, position 94,219,175. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

MRE11Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:94219175
Cytoband
11q21
HGVS
NM_005591.4(MRE11):c.229G>T (p.Glu77Ter)
Allele change
Nonsense_E77X

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Ataxia-telangiectasia-like disorder

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.