Variant (rsID / SNP)

rs338599

rs338599 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2S1. Location: chromosome 19, position 41,700,493. The table records no clinical significance for this variant.

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Reference-table entries

CYP2S1Not classified

Variant type: synonymous_variant
Chromosome / position: 19:41700493
HGVS: NM_030622.8,c.222G>C,p.Pro74Pro
Allele change: Synonymous_P74P

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.