Gene entry
FIG4
FIG4 phosphoinositide 5-phosphatase
- Chromosome
- 6
- Cytoband
- 6q21
- Variants (rsID)
- 26
FIG4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6q21). Its official name is “FIG4 phosphoinositide 5-phosphatase”. The reference table lists 26 variants (rsID) for this gene.
Clinically classified variants
10 reference-table entries with clinical significance.
- rs1127771Benignsingle nucleotide variantAmyotrophic lateral sclerosis type 11|Charcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease|Charcot-Marie-Tooth disease type 4J|Yunis-Varon syndrome|Bilateral parasagittal parieto-occipital polymicrogyria
- rs145337669Benignsingle nucleotide variantAmyotrophic lateral sclerosis type 11|Charcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4J
- rs61729092Benignsingle nucleotide variantAmyotrophic lateral sclerosis type 11|Charcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4J|Charcot-Marie-Tooth disease
- rs9885672Benignsingle nucleotide variantCharcot-Marie-Tooth disease type 4|Amyotrophic lateral sclerosis type 11|Charcot-Marie-Tooth disease type 4J|Charcot-Marie-Tooth disease|Yunis-Varon syndrome|Bilateral parasagittal parieto-occipital polymicrogyria
- rs121908287Conflicting interpretationssingle nucleotide variantCharcot-Marie-Tooth disease type 4J|Amyotrophic lateral sclerosis type 11|Charcot-Marie-Tooth disease type 4|Amyotrophic lateral sclerosis|Yunis-Varon syndrome|Bilateral parasagittal parieto-occipital polymicrogyria|Charcot-Marie-Tooth disease type 4J|Yunis-Varon syndrome|FIG4-Related Disorders
- rs142482745Conflicting interpretationssingle nucleotide variantCharcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4J|Amyotrophic lateral sclerosis type 11|Charcot-Marie-Tooth disease
- rs200267243Conflicting interpretationssingle nucleotide variantAmyotrophic lateral sclerosis type 11|Charcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4J|Charcot-Marie-Tooth disease
- rs121908288Pathogenicsingle nucleotide variantAmyotrophic lateral sclerosis type 11|Charcot-Marie-Tooth disease type 4J|Charcot-Marie-Tooth disease type 4|Amyotrophic lateral sclerosis
- rs377357931Pathogenicsingle nucleotide variantCharcot-Marie-Tooth disease type 4J|Inborn genetic diseases|Charcot-Marie-Tooth disease type 4
- rs138376077Uncertain significancesingle nucleotide variantCharcot-Marie-Tooth disease type 4
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.