Gene entry
FGF12
fibroblast growth factor 12
- Chromosome
- 3
- Cytoband
- 3q28-q29
- Variants (rsID)
- 228
FGF12 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q28-q29). Its official name is “fibroblast growth factor 12”. The reference table lists 228 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs886039903Pathogenicsingle nucleotide variantDevelopmental and epileptic encephalopathy, 47|Early onset epileptic encephalopathy
Other listed variants
- rs781403
- rs781411
- rs781416
- rs781417
- rs781418
- rs781422
- rs796676
- rs809714
- rs923818
- rs923819
- rs940901
- rs975121
- rs989512
- rs1393989
- rs1464507
- rs1501621
- rs1501622
- rs1503592
- rs1522264
- rs1532684
- rs1847340
- rs1875455
- rs1875733
- rs1910882
- rs1922910
- rs1922911
- rs1961246
- rs1995472
- rs2047857
- rs2049212
- rs2253098
- rs2253332
- rs2292160
- rs2293147
- rs2366664
- rs2366688
- rs2366691
- rs2654693
- rs2654699
- rs2669297
- rs2692700
- rs2708308
- rs2710776
- rs2710779
- rs2886705
- rs3106408
- rs3108301
- rs3108303
- rs3109182
- rs3109183
- rs3109185
- rs4234623
- rs4279038
- rs4299433
- rs4434103
- rs4453795
- rs4580495
- rs4687301
- rs4687322
- rs4687344
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
