Variant (rsID / SNP)

rs61743864

rs61743864 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COQ6. Location: chromosome 14, position 74,420,252. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

COQ6Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 14:74420252
Cytoband: 14q24.3
HGVS: NM_182476.3(COQ6):c.278G>A (p.Gly93Asp)
Allele change: Missense_G68D

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.