What is a “Variant of Uncertain Significance (VUS)”—and What Should You Do About It?

Getting a genetic test result can feel overwhelming—especially when you see a term like “Variant of Uncertain Significance” (VUS). If you’ve received a VUS result, the good news is this: it does not mean you have a disease, and it does not automatically mean your family members are at risk.

Let’s break it down simply.


What is a VUS?

A variant is a small difference in your DNA. Everyone has thousands of genetic variants—most are harmless and simply make us unique.

A Variant of Uncertain Significance (VUS) means:

  • A change was found in a gene, but
  • Scientists do not yet have enough evidence to say whether it is:
    • harmless (benign), or
    • disease-causing (pathogenic)

In short, a VUS is a genetic finding that is still “under study.”

Why does a VUS happen?

A VUS result is common, especially when more genes are tested (like in exome or genome sequencing). It can happen because:

  • Not enough people with the same variant have been studied yet
  • The variant is rare, and there’s limited global data
  • Different populations may have different normal genetic patterns
  • We don’t fully understand every part of every gene (yet)

Genetics is advancing quickly, but some answers take time.

Does a VUS mean I will get a genetic disease?

No. Not necessarily.

A VUS is not a confirmed diagnosis. Many VUS results later turn out to be benign (harmless). Some may later be confirmed as disease-causing, but until that happens, it remains uncertain.

This is why doctors usually do not make major medical decisions based on a VUS alone.

What should you do if your report shows a VUS?

Here are the most helpful and practical steps:

1) Don’t panic—and don’t assume the worst

A VUS is best understood as:
“We found something, but we don’t know what it means yet.”

It is not the same as a positive result.

2) Discuss the result with a genetic counselor or specialist

A genetic counselor can explain:

  • what the gene is related to
  • whether your symptoms match the condition linked to that gene
  • whether this VUS is likely to be important or not

They can also guide your next steps safely.

3) Do not change treatment or undergo surgery based only on a VUS

In most cases, a VUS should not lead to decisions like:

  • preventive surgery
  • stopping a medication
  • major long-term treatment changes

Your doctor will consider your personal medical history, symptoms, and family history first.

4) Review your family history carefully

Even if a VUS is uncertain, your family history can still provide clear risk clues.

For example:

  • multiple relatives with early cancer
  • repeated miscarriages or genetic conditions in the family
  • similar symptoms in close relatives

Sometimes, your doctor may recommend screening or follow-up based on family history alone.

5) In some cases, family testing may help

Your healthcare team may suggest testing certain family members to see whether the VUS:

  • is present in relatives with the condition, or
  • is also found in healthy relatives

This can provide clues—but it doesn’t always give a final answer.

6) Ask about reclassification (future updates)

One important fact: a VUS can be reclassified over time as more research becomes available.

It may later become:

  • Benign / Likely benign (harmless), or
  • Pathogenic / Likely pathogenic (disease-causing)

Ask your testing lab or doctor:

  • “Will I be informed if this VUS is reclassified?”
  • “Should I follow up again in 1–2 years?”

The key message to remember

A VUS is not a diagnosis.
It is a “maybe” result that requires more evidence.

What matters most right now is:

  • your symptoms (if any)
  • your medical history
  • your family history
  • guidance from your doctor or genetic counselor

When should you seek help urgently?

You should follow up promptly if:

  • you have strong symptoms and no diagnosis yet
  • there is a strong family history of inherited disease
  • the report includes other findings besides the VUS
  • you feel anxious and need clear guidance (this is very common)

Final reassurance

Genetic testing is a powerful tool, but not every result gives an immediate clear answer. A VUS simply reflects where science is today—not something you did wrong, and not something you should fear.

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