Variant (rsID / SNP)

rs987495

rs987495 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFI44L. Location: chromosome 1, position 79,095,581. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

IFI44LNot classified

Variant type: missense_variant
Chromosome / position: 1:79095581
HGVS: NM_001375646.1,c.704T>C,p.Ile235Thr
Allele change: Missense_I235T

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.