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Variant (rsID / SNP)

rs4787643

SEPTIN1

rs4787643 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEPTIN1. Location: chromosome 16, position 30,393,660. The table records no clinical significance for this variant.

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Reference-table entries

SEPTIN1Not classified
Variant type
synonymous_variant
Chromosome / position
16:30393660
HGVS
NM_001365977.2,c.45C>T,p.Ala15Ala
Allele change
Synonymous_A57A

Public references

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