GENE REFERENCE / HGNC:45010

WASHC2EP

WASHC2E, pseudogene

pseudogene10q11.23Basic gene details

What does this gene do?

The MedlinePlus data used here does not include an explanation of what this gene does. Its name and other identifying details come from HGNC.

ClinGen reviews

We found no matching ClinGen review in the data used here. This does not rule out a link between the gene and a condition.

ClinVar records

We found no matching entry in the ClinVar gene summary used here. This does not mean that every variant in the gene is harmless.

YOUR DNA FILE

Can your DNA file tell you about WASHC2EP?

From a DNA test kit (such as 23andMe, AncestryDNA or MyHeritage). These kits check a fixed list of about 600,000 to 700,000 positions across your whole genome.

From whole genome sequencing (a VCF file). Sequencing reads most of your genome. Your file lists the places where your DNA differs from the reference genome. Some regions are hard to sequence, including parts of some genes that have near-identical copies elsewhere, and a VCF file does not record which positions were read well.

If a variant is not in your file, that does not mean you don’t have it.

What BioDecode checks

BioDecode compares every variant in your file with ClinVar, on your own computer. For each match, it shows the ClinVar classification, the review status and the condition it was reported for. Your file is not uploaded.

A ClinVar classification applies to one particular variant and the condition it was reported for. It does not tell you about other variants in WASHC2EP.

BioDecode cannot fill gaps in your test, diagnose a condition or replace clinical testing.

Buy BioDecode See a sample report →Check file compatibility →