Variant (rsID / SNP)

rs377109096

rs377109096 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MT-ND4. Clinical significance in the table: Likely benign.

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Reference-table entries

MT-ND4Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Cytoband: -
HGVS: NC_012920.1:m.11167A>G

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.