Variant (rsID / SNP)

rs28509789

rs28509789 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C15ORF39, C15orf39. Location: chromosome 15, position 75,499,995. The table records no clinical significance for this variant.

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Reference-table entries

C15ORF39Not classified

Variant type: missense_variant
Chromosome / position: 15:75499995
HGVS: NM_015492.5,c.1606T>G,p.Ser536Ala
Allele change: Missense_S536A

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.