Variant (rsID / SNP)

rs313838

rs313838 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRKD2. Location: chromosome 19, position 47,221,129. The table records no clinical significance for this variant.

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Reference-table entries

PRKD2Not classified

Variant type: upstream_gene_variant
Chromosome / position: 19:47221129
HGVS: NM_001079880.2,c.-1223C>T

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.