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Variant (rsID / SNP)

rs3745990

FSD1

rs3745990 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FSD1. Location: chromosome 19, position 4,318,365. The table records no clinical significance for this variant.

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Reference-table entries

FSD1Not classified
Variant type
synonymous_variant
Chromosome / position
19:4318365
HGVS
NM_024333.3,c.822G>A,p.Ala274Ala
Allele change
Synonymous_A274A

Public references

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