Variant (rsID / SNP)

rs35732034

rs35732034 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFIH1. Location: chromosome 2, position 163,124,596. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

IFIH1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:163124596
Cytoband: 2q24.2
HGVS: NM_022168.4(IFIH1):c.2807+1G>A
Allele change: Silent

Associated conditions / phenotypes

Aicardi-Goutieres syndrome 7|Singleton-Merten syndrome 1|Immunodeficiency 95

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.