Variant (rsID / SNP)

rs371077728

rs371077728 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRE11. Location: chromosome 11, position 94,200,987. Clinical significance in the table: Uncertain significance.

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Reference-table entries

MRE11Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 11:94200987
Cytoband: 11q21
HGVS: NM_005591.4(MRE11):c.1090C>G (p.Arg364Gly)
Allele change: Nonsense_R364X

Associated conditions / phenotypes

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

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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