Definition

Heterozygous pathogenic variants in the HNF1A gene impair the activity of a transcription factor that regulates genes directing beta cell development and function. HNF1A-MODY is the most common subtype, accounting for 50 to 70% of all MODY cases; findings generally appear before age 30, and sensitivity to sulfonylureas is preserved.

Gene/region analyzed

HNF1A - Exon 1, HNF1A - Exon 2, HNF1A - Exon 3, HNF1A - Exon 4, HNF1A - Exon 5, HNF1A - Exon 6, HNF1A - Exon 7, HNF1A - Exon 8, HNF1A - Exon 9, HNF1A - Exon 10

Method

Sequence analysis

Accepted sample types

EDTA blood, AF, CVS

Inheritance

Hereditary, autosomal dominant.

Related Tests

Inheritance Patterns

Describes how a genetic condition is passed on within a family. There are five main patterns

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Carrier (Heterozygous / Homozygous)

Why it matters: In autosomal recessive inheritance, when each parent is a carrier (while both appear healthy), the chance of their child being born with the disease is 25% in each

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VUS (Variant of Uncertain Significance)

This is the situation where the test has detected a change in the DNA, but the role of this change in the development of disease is unconfirmed.

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How to Read a Genetic Test Result (Positive / Negative / VUS)

A genetic test result falls into three main categories

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Types of Genetic Tests

A genetic test is a type of medical test that detects changes in genes, chromosomes or proteins. Today there are more than 77,000 genetic tests available.

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