Gene entry
GPC3
glypican 3
- Chromosome
- X
- Cytoband
- Xq26.2
- Variants (rsID)
- 43
GPC3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq26.2). Its official name is “glypican 3”. The reference table lists 43 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs11539789Benignsingle nucleotide variantHistory of neurodevelopmental disorder|Wilms tumor 1
- rs2314298Benignsingle nucleotide variantWilms tumor 1|History of neurodevelopmental disorder|Hereditary cancer-predisposing syndrome
- rs138450923Conflicting interpretationssingle nucleotide variantHistory of neurodevelopmental disorder|Wilms tumor 1
- rs141100113Conflicting interpretationssingle nucleotide variantHistory of neurodevelopmental disorder|Wilms tumor 1|Hereditary cancer-predisposing syndrome
- rs745968470Conflicting interpretationssingle nucleotide variantWilms tumor 1
- rs122453119Pathogenicsingle nucleotide variantWilms tumor 1
- rs122453121Pathogenicsingle nucleotide variantSimpson-Golabi-Behmel syndrome type 1|Wilms tumor 1
- rs122453120Uncertain significancesingle nucleotide variantWilms tumor 1
Other listed variants
- rs879941
- rs1003856
- rs1264379
- rs1264380
- rs2132717
- rs2267514
- rs2267520
- rs2267527
- rs2284125
- rs4829762
- rs4830273
- rs5933330
- rs5933362
- rs5975428
- rs5977893
- rs5977901
- rs6634941
- rs7876682
- rs7877771
- rs12558298
- rs12687021
- rs13440964
- rs17251516
- rs17277770
- rs72615418
- rs73241304
- rs138300873
- rs138799073
- rs140304018
- rs142124613
- rs143374146
- rs144416314
- rs145860493
- rs146192779
- rs151239422
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.