Variant (rsID / SNP)

rs1799841

rs1799841 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CST5. Location: chromosome 20, position 23,860,178. The table records no clinical significance for this variant.

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Reference-table entries

CST5Not classified

Variant type: missense_variant
Chromosome / position: 20:23860178
HGVS: NM_001900.5,c.136T>C,p.Cys46Arg
Allele change: Missense_C46R

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.