Variant (rsID / SNP)

rs28368158

rs28368158 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFNA16. Location: chromosome 9, position 21,217,166. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

IFNA16Not classified

Variant type: missense_variant
Chromosome / position: 9:21217166
HGVS: NM_002173.3,c.139A>G,p.Ile47Val
Allele change: Missense_I47V

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.