Variant (rsID / SNP)

rs73592448

rs73592448 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PROSER3. Location: chromosome 19, position 36,258,721. The table records no clinical significance for this variant.

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Reference-table entries

PROSER3Not classified

Variant type: missense_variant
Chromosome / position: 19:36258721
HGVS: NM_001367856.1,c.1706C>T,p.Ala569Val
Allele change: Missense_A325V

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.