Gene entry
FLNB
filamin B
- Chromosome
- 3
- Cytoband
- 3p14.3
- Variants (rsID)
- 63
FLNB is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p14.3). Its official name is “filamin B”. The reference table lists 63 variants (rsID) for this gene.
Clinically classified variants
20 reference-table entries with clinical significance.
- rs111330368Benignsingle nucleotide variantFLNB-Related Spectrum Disorders|Connective tissue disorder
- rs1131356Benignsingle nucleotide variantFLNB-Related Spectrum Disorders
- rs116826041Benignsingle nucleotide variantFLNB-Related Spectrum Disorders|Larsen syndrome|Connective tissue disorder
- rs12632456Benignsingle nucleotide variantFLNB-Related Spectrum Disorders
- rs138327769Benignsingle nucleotide variantFLNB-Related Spectrum Disorders
- rs2362904Benignsingle nucleotide variantFLNB-Related Spectrum Disorders
- rs377095569Benignsingle nucleotide variantFLNB-Related Spectrum Disorders
- rs62621996Benignsingle nucleotide variantFLNB-Related Spectrum Disorders|Connective tissue disorder
- rs9809281Benignsingle nucleotide variant
- rs9813235Benignsingle nucleotide variant
- rs9826147Benignsingle nucleotide variant
- rs13321615Conflicting interpretationssingle nucleotide variantFLNB-Related Spectrum Disorders|Connective tissue disorder
- rs137885421Conflicting interpretationssingle nucleotide variantFLNB-Related Spectrum Disorders
- rs138220431Conflicting interpretationssingle nucleotide variantFLNB-Related Spectrum Disorders
- rs139846706Conflicting interpretationssingle nucleotide variantConnective tissue disorder
- rs142568031Conflicting interpretationssingle nucleotide variantConnective tissue disorder
- rs150445941Conflicting interpretationssingle nucleotide variantFLNB-Related Spectrum Disorders|Connective tissue disorder
- rs151259375Conflicting interpretationssingle nucleotide variantFLNB-Related Spectrum Disorders
- rs202143851Conflicting interpretationssingle nucleotide variantFLNB-Related Spectrum Disorders
- rs80356517Pathogenicsingle nucleotide variantSpondylocarpotarsal synostosis syndrome
Other listed variants
- rs704529
- rs839225
- rs839231
- rs1658351
- rs2276742
- rs4681784
- rs6764184
- rs7430045
- rs9828717
- rs9836278
- rs9856128
- rs11130613
- rs11714241
- rs13077017
- rs35997722
- rs56697644
- rs60183346
- rs74824935
- rs75895354
- rs79495046
- rs114002304
- rs138034708
- rs139664696
- rs141342605
- rs141559684
- rs145526641
- rs146573525
- rs146583950
- rs146685642
- rs149600652
- rs187669646
- rs189785975
- rs199513147
- rs199760437
- rs200619215
- rs201030123
- rs201165196
- rs201254275
- rs201533113
- rs201630300
- rs201852092
- rs201882876
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.