Variant (rsID / SNP)

rs2824751

rs2824751 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMPRSS15. Location: chromosome 21, position 19,713,821. The table records no clinical significance for this variant.

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Reference-table entries

TMPRSS15Not classified

Variant type: synonymous_variant
Chromosome / position: 21:19713821
HGVS: NM_002772.3,c.1473G>A,p.Ala491Ala
Allele change: Synonymous_A491A

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.