Variant (rsID / SNP)

rs8289

rs8289 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLIN3. Location: chromosome 19, position 4,859,937. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PLIN3Not classified

Variant type: missense_variant
Chromosome / position: 19:4859937
HGVS: NM_005817.5,c.166A>G,p.Ile56Val
Allele change: Missense_I56V

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.