Variant (rsID / SNP)

rs35318931

rs35318931 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SRPX. The table records no clinical significance for this variant.

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Reference-table entries

SRPXNot classified

Variant type: missense_variant
HGVS: NM_006307.5,c.1238C>T,p.Ser413Phe
Allele change: Missense_S393F

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.