Variant (rsID / SNP)

rs560219

rs560219 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STPG1. Location: chromosome 1, position 24,718,079. The table records no clinical significance for this variant.

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Reference-table entries

STPG1Not classified

Variant type: missense_variant
Chromosome / position: 1:24718079
HGVS: NM_001199012.2,c.161G>T,p.Ser54Ile
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.