Variant (rsID / SNP)

rs73516829

rs73516829 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCSK4. Location: chromosome 19, position 1,490,285. The table records no clinical significance for this variant.

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Reference-table entries

PCSK4Not classified

Variant type: missense_variant
Chromosome / position: 19:1490285
HGVS: NM_017573.5,c.61C>T,p.Pro21Ser
Allele change: Missense_P21S

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.