Variant (rsID / SNP)

rs121434475

rs121434475 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MT-TG, MT-CO3. Clinical significance in the table: Uncertain significance.

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Reference-table entries

MT-TGUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Cytoband: -
HGVS: m.9997T>C

Associated conditions / phenotypes

Primary familial hypertrophic cardiomyopathy

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.