Variant (rsID / SNP)

rs62621173

rs62621173 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFI16. Location: chromosome 1, position 159,021,506. The table records no clinical significance for this variant.

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Reference-table entries

IFI16Not classified

Variant type: missense_variant
Chromosome / position: 1:159021506
HGVS: NM_001364867.2,c.1703C>T,p.Ser568Phe
Allele change: Missense_S568F

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.