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Variant (rsID / SNP)

rs1048013

CYP20A1

rs1048013 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP20A1. Location: chromosome 2, position 204,154,552. The table records no clinical significance for this variant.

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Reference-table entries

CYP20A1Not classified
Variant type
missense_variant
Chromosome / position
2:204154552
HGVS
NM_001371695.1,c.1060C>T,p.Leu354Phe
Allele change
Missense_L346F

Public references

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