Variant (rsID / SNP)

rs2303652

rs2303652 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DEDD2. Location: chromosome 19, position 42,703,833. The table records no clinical significance for this variant.

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Reference-table entries

DEDD2Not classified

Variant type: synonymous_variant
Chromosome / position: 19:42703833
HGVS: NM_001270614.2,c.738T>C,p.Ser246Ser
Allele change: Silent

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.