Variant (rsID / SNP)

rs1023000

rs1023000 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FNBP1. Location: chromosome 9, position 132,662,786. The table records no clinical significance for this variant.

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Reference-table entries

FNBP1Not classified

Variant type: missense_variant
Chromosome / position: 9:132662786
HGVS: NM_015033.3,c.1469G>A,p.Ser490Asn
Allele change: Missense_S490N

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.