Variant (rsID / SNP)

rs2229207

rs2229207 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFNAR2. Location: chromosome 21, position 34,614,250. Clinical significance in the table: Benign.

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Reference-table entries

IFNAR2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 21:34614250
Cytoband: 21q22.11
HGVS: NM_001289125.3(IFNAR2):c.23T>C (p.Phe8Ser)
Allele change: Missense_F8S

Associated conditions / phenotypes

Hepatitis B virus, susceptibility to|Immunodeficiency 45

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.