Variant (rsID / SNP)

rs1727

rs1727 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFIT2. Location: chromosome 10, position 91,066,769. The table records no clinical significance for this variant.

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Reference-table entries

IFIT2Not classified

Variant type: missense_variant
Chromosome / position: 10:91066769
HGVS: NM_001547.5,c.1056C>A,p.Asp352Glu
Allele change: Missense_D352E

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.