Variant (rsID / SNP)

rs527236193

rs527236193 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MT-CYB. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MT-CYBBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: -
HGVS: NC_012920.1:m.15758A>G

Associated conditions / phenotypes

Familial cancer of breast|Leigh syndrome

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.