Variant (rsID / SNP)

rs201395766

rs201395766 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MT-CO1. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MT-CO1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Cytoband: -
HGVS: NC_012920.1(MT-CO1):m.6260G>A

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.