Variant (rsID / SNP)

rs112963053

rs112963053 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFNA10. Location: chromosome 9, position 21,206,743. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

IFNA10Not classified

Variant type: missense_variant
Chromosome / position: 9:21206743
HGVS: NM_002171.2,c.354C>A,p.Asp118Glu
Allele change: Missense_D118E

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.