Variant (rsID / SNP)

rs28445203

rs28445203 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MT-RNR2, MT-ND1. Clinical significance in the table: Uncertain significance.

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Reference-table entries

MT-RNR2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Cytoband: -
HGVS: NC_012920.1:m.2483T>C
Allele change: Silent

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.