Variant (rsID / SNP)

rs4968839

rs4968839 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCA6. Location: chromosome 17, position 67,125,840. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ABCA6Not classified

Variant type: missense_variant
Chromosome / position: 17:67125840
HGVS: NM_080284.3,c.844G>A,p.Val282Ile
Allele change: Missense_V282I

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.