Resources & support

Where to go from here

GeneTranslate is an educational starting point. The real conversation is with a board-certified counselor. Below are vetted directories, plain-language education, and patient support communities to help you take the next step.

Find a genetic counselor

A counseling appointment is the right next step after any positive or uncertain finding.

Patient education

Trusted, free resources for understanding your condition and its inheritance.

Understanding ACMG variant classes

Labs use a 5-tier system to rate how confident they are that a variant causes disease. Classifications can change as new evidence emerges — ask your counselor whether a reclassification is worth checking.

Pathogenic

Strong evidence the variant causes disease.

Likely pathogenic

Evidence leans toward disease-causing but isn't definitive.

Variant of uncertain significance

Not enough evidence yet to classify either way. Often reclassified later.

Likely benign

Evidence leans toward harmless.

Benign

Strong evidence the variant does not cause disease.

Support communities

Receiving genetic results can be overwhelming. These communities offer peer support, advocacy, and patient resources.

Have feedback or a question?

GeneTranslate is open and ephemeral — we don’t track usage or hold accounts. For product feedback, bug reports, or to ask us to support a new lab format, email support@genetranslate.example.

Please do not include real patient data, PHI, or report PDFs in support emails.

Looking for product help? Try the FAQ or how it works.