Variant (rsID / SNP)

rs4915221

rs4915221 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGFN1. Location: chromosome 1, position 201,166,383. The table records no clinical significance for this variant.

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Reference-table entries

IGFN1Not classified

Variant type: missense_variant
Chromosome / position: 1:201166383
HGVS: NM_001164586.2,c.305G>A,p.Arg102His
Allele change: Missense_R102H

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.