Variant (rsID / SNP)

rs4807578

rs4807578 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FSD1. Location: chromosome 19, position 4,306,311. The table records no clinical significance for this variant.

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Reference-table entries

FSD1Not classified

Variant type: synonymous_variant
Chromosome / position: 19:4306311
HGVS: NM_024333.3,c.228T>C,p.Arg76Arg
Allele change: Synonymous_R76R

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.