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Variant (rsID / SNP)

rs35667974

IFIH1

rs35667974 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFIH1. Location: chromosome 2, position 163,124,637. 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
2:163124637
Cytoband
2q24.2
HGVS
NM_022168.4(IFIH1):c.2767A>G (p.Ile923Val)
Allele change
Missense_I923V

Associated conditions / phenotypes

Aicardi-Goutieres syndrome 7|Singleton-Merten syndrome 1

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.