Gene entry
SBF2
SET binding factor 2
- Chromosome
- 11
- Cytoband
- 11p15.4
- Variants (rsID)
- 94
SBF2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11p15.4). Its official name is “SET binding factor 2”. The reference table lists 94 variants (rsID) for this gene.
Clinically classified variants
15 reference-table entries with clinical significance.
- rs10118Benignsingle nucleotide variantCharcot-Marie-Tooth disease type 4B2
- rs140730386Benignsingle nucleotide variantCharcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4B2|Charcot-Marie-Tooth disease
- rs148187321Benignsingle nucleotide variantCharcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4B2
- rs16907355Benignsingle nucleotide variantCharcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4B2|Charcot-Marie-Tooth disease
- rs79470805Benignsingle nucleotide variantCharcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4B2|Charcot-Marie-Tooth disease
- rs139967004Conflicting interpretationssingle nucleotide variantCharcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4B2
- rs141330687Conflicting interpretationssingle nucleotide variantCharcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4B2|Charcot-Marie-Tooth disease|Toe walking
- rs141894081Conflicting interpretationssingle nucleotide variantCharcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4B2|Charcot-Marie-Tooth disease|Toe walking
- rs143209062Conflicting interpretationssingle nucleotide variantCharcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease|Charcot-Marie-Tooth disease type 4B2
- rs143773975Conflicting interpretationssingle nucleotide variantCharcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4B2|Charcot-Marie-Tooth disease
- rs145351367Conflicting interpretationssingle nucleotide variantCharcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4B2|Charcot-Marie-Tooth disease
- rs200784979Conflicting interpretationssingle nucleotide variantCharcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4B2|Charcot-Marie-Tooth disease
- rs761285505Conflicting interpretationssingle nucleotide variantCharcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4B2
- rs138120231Uncertain significancesingle nucleotide variantCharcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4B2|Charcot-Marie-Tooth disease
- rs188588431Uncertain significancesingle nucleotide variantCharcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease
Other listed variants
- rs360168
- rs360169
- rs421752
- rs780382
- rs1442740
- rs1470260
- rs2119991
- rs2278631
- rs2645013
- rs4910508
- rs7106234
- rs7939451
- rs7950655
- rs9919621
- rs9971507
- rs10500716
- rs10500717
- rs11042605
- rs11042639
- rs11042669
- rs11600251
- rs12283105
- rs12288275
- rs12796169
- rs17272637
- rs34509215
- rs35103525
- rs56037770
- rs56374204
- rs61129164
- rs61876909
- rs61877052
- rs61889797
- rs66922162
- rs71476850
- rs72853260
- rs72853268
- rs72858826
- rs72861742
- rs73412899
- rs74498276
- rs74594145
- rs75320405
- rs75920705
- rs75948396
- rs76130421
- rs76674358
- rs77049148
- rs77183865
- rs77540235
- rs77883822
- rs78896333
- rs78959883
- rs79630589
- rs80110426
- rs111471011
- rs112022101
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
