Variant (rsID / SNP)

rs9651057

rs9651057 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGFN1. Location: chromosome 1, position 201,175,274. The table records no clinical significance for this variant.

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Reference-table entries

IGFN1Not classified

Variant type: missense_variant
Chromosome / position: 1:201175274
HGVS: NM_001164586.2,c.1253A>G,p.Gln418Arg
Allele change: Missense_Q418R

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.