Variant (rsID / SNP)

rs320995

rs320995 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYSLTR1. The table records no clinical significance for this variant.

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Reference-table entries

CYSLTR1Not classified

Variant type: synonymous_variant
HGVS: NM_001282186.2,c.927C>T,p.Phe309Phe
Allele change: Synonymous_F309F

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.