Variant (rsID / SNP)

rs207460001

rs207460001 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MT-CYB. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MT-CYBPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Cytoband: -
HGVS: m.15197T>C

Associated conditions / phenotypes

Exercise intolerance

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.