Gene entry
RAB3GAP1
RAB3 GTPase activating protein catalytic subunit 1
- Chromosome
- 2
- Cytoband
- 2q21.3
- Variants (rsID)
- 18
RAB3GAP1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q21.3). Its official name is “RAB3 GTPase activating protein catalytic subunit 1”. The reference table lists 18 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs114901298Benignsingle nucleotide variantWarburg micro syndrome 1
- rs116775947Benignsingle nucleotide variantWarburg micro syndrome 1
- rs150478342Benignsingle nucleotide variantWarburg micro syndrome 1|Amenorrhea
- rs17261772Benignsingle nucleotide variantWarburg micro syndrome|Warburg micro syndrome 1|Martsolf syndrome 2
- rs61748693Benignsingle nucleotide variantWarburg micro syndrome 1
- rs76927619Benignsingle nucleotide variantWarburg micro syndrome 1
- rs140929274Conflicting interpretationssingle nucleotide variantWarburg micro syndrome 1
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.