Variant (rsID / SNP)

rs118203890

rs118203890 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MT-TT. Clinical significance in the table: Uncertain significance.

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Reference-table entries

MT-TTUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Cytoband: -
HGVS: m.15950G>A

Associated conditions / phenotypes

Parkinson disease, mitochondrial|Juvenile myopathy, encephalopathy, lactic acidosis AND stroke

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.