Gene entry
GLDC
glycine decarboxylase
- Chromosome
- 9
- Cytoband
- 9p24.1
- Variants (rsID)
- 60
GLDC is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9p24.1). Its official name is “glycine decarboxylase”. The reference table lists 60 variants (rsID) for this gene.
Clinically classified variants
26 reference-table entries with clinical significance.
- rs141014950Benignsingle nucleotide variantNon-ketotic hyperglycinemia
- rs143119940Benignsingle nucleotide variantNon-ketotic hyperglycinemia
- rs73639325Benignsingle nucleotide variantNon-ketotic hyperglycinemia
- rs7848919Benignsingle nucleotide variantNon-ketotic hyperglycinemia
- rs138640017Conflicting interpretationssingle nucleotide variantNon-ketotic hyperglycinemia
- rs151268759Conflicting interpretationssingle nucleotide variantNon-ketotic hyperglycinemia
- rs201135624Conflicting interpretationssingle nucleotide variantNon-ketotic hyperglycinemia|Smith-Magenis Syndrome-like
- rs386833551Conflicting interpretationssingle nucleotide variantNon-ketotic hyperglycinemia
- rs386833536Likely pathogenicsingle nucleotide variantNon-ketotic hyperglycinemia
- rs386833576Likely pathogenicsingle nucleotide variantNon-ketotic hyperglycinemia
- rs121964974Pathogenicsingle nucleotide variantNon-ketotic hyperglycinemia
- rs121964976Pathogenicsingle nucleotide variantNon-ketotic hyperglycinemia|Generalized epilepsy|Global developmental delay|Obesity
- rs121964979Pathogenicsingle nucleotide variantNon-ketotic hyperglycinemia
- rs121964980Pathogenicsingle nucleotide variantNon-ketotic hyperglycinemia
- rs149070244Pathogenicsingle nucleotide variantNon-ketotic hyperglycinemia
- rs188269735Pathogenicsingle nucleotide variantNon-ketotic hyperglycinemia
- rs191905539Pathogenicsingle nucleotide variantNon-ketotic hyperglycinemia|Inborn genetic diseases
- rs386833517Pathogenicsingle nucleotide variantNon-ketotic hyperglycinemia
- rs386833549Pathogenicsingle nucleotide variantNon-ketotic hyperglycinemia
- rs386833555Pathogenicsingle nucleotide variantNon-ketotic hyperglycinemia
- rs386833560Pathogenicsingle nucleotide variantNon-ketotic hyperglycinemia
- rs386833585Pathogenicsingle nucleotide variantNon-ketotic hyperglycinemia
- rs140411475Uncertain significancesingle nucleotide variantNon-ketotic hyperglycinemia
- rs150624881Uncertain significancesingle nucleotide variantNon-ketotic hyperglycinemia
- rs200413149Uncertain significancesingle nucleotide variantNon-ketotic hyperglycinemia
- rs386833571Uncertain significancesingle nucleotide variantNon-ketotic hyperglycinemia
Other listed variants
- rs934854
- rs1658953
- rs2118654
- rs2282158
- rs4333664
- rs4512434
- rs4742234
- rs7021684
- rs7031908
- rs7034327
- rs7870809
- rs10124449
- rs10511461
- rs10815447
- rs10975641
- rs11999777
- rs12347456
- rs13295349
- rs16924682
- rs16924709
- rs35974452
- rs41281769
- rs45582831
- rs55645178
- rs62568964
- rs62568995
- rs74349587
- rs78533019
- rs80147714
- rs117035473
- rs117199224
- rs117225298
- rs117538488
- rs191053099
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
