Variant (rsID / SNP)

rs35646566

rs35646566 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SERPIND1. Location: chromosome 22, position 21,134,023. The table records no clinical significance for this variant.

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Reference-table entries

SERPIND1Not classified

Variant type: synonymous_variant
Chromosome / position: 22:21134023
HGVS: NM_000185.4,c.423G>A,p.Leu141Leu
Allele change: Silent

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.