Variant (rsID / SNP)

rs2824790

rs2824790 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMPRSS15. Location: chromosome 21, position 19,756,040. The table records no clinical significance for this variant.

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Reference-table entries

TMPRSS15Not classified

Variant type: missense_variant
Chromosome / position: 21:19756040
HGVS: NM_002772.3,c.400G>C,p.Glu134Gln
Allele change: Missense_E134Q

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.