Variant (rsID / SNP)

rs4842

rs4842 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP5PO. Location: chromosome 21, position 35,281,421. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ATP5PONot classified

Variant type: missense_variant
Chromosome / position: 21:35281421
HGVS: NM_001697.3,c.293A>G,p.Lys98Arg
Allele change: Missense_K98R

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.