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Variant (rsID / SNP)

rs20543

PCSK6

rs20543 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCSK6. Location: chromosome 15, position 101,910,550. The table records no clinical significance for this variant.

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Reference-table entries

PCSK6Not classified
Variant type
synonymous_variant
Chromosome / position
15:101910550
HGVS
NM_002570.5,c.1708C>T,p.Leu570Leu
Allele change
Missense_S570F

Associated conditions / phenotypes

Missense_S570F

Public references

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