Gene entry
SYNE2
spectrin repeat containing nuclear envelope protein 2
- Chromosome
- 14
- Cytoband
- 14q23.2
- Variants (rsID)
- 117
SYNE2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q23.2). Its official name is “spectrin repeat containing nuclear envelope protein 2”. The reference table lists 117 variants (rsID) for this gene.
Clinically classified variants
58 reference-table entries with clinical significance.
- rs10133691Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs10137972Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs10151658Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs1048315Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs11628107Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs117070973Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs11847087Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs12881815Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs138689053Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs142000273Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs142277402Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs142660236Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs146748294Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs150955173Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs17101637Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs17179194Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs17751301Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs1890908Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs2297301Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs34944385Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs35203186Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs3829767Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs61747118Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs7161192Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs75568433Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs76634907Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs8010699Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs9944035Benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs117647282Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs138514054Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs138769395Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy|Emery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs138789938Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs140897155Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs141488398Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs143578863Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs144596211Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs144599409Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs145036293Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs146573874Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs148323208Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs148492034Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs149227847Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs149354607Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs149978500Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs187859624Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs192128801Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs199561218Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs199566869Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs199577239Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs200742016Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs200937358Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs201427580Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs551801857Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs74975380Conflicting interpretationssingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs200893937Likely benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs200971467Likely benignsingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs199976741Uncertain significancesingle nucleotide variantEmery-Dreifuss muscular dystrophy 5, autosomal dominant
- rs1255953Not classifiedintron_variant
Other listed variants
- rs963289
- rs1152584
- rs1255989
- rs2781426
- rs3031361
- rs3915546
- rs4902243
- rs7144688
- rs7144722
- rs7153036
- rs7157314
- rs7157785
- rs8003797
- rs8013611
- rs9919904
- rs10135310
- rs10149314
- rs11848293
- rs11849690
- rs12589129
- rs12883524
- rs12891546
- rs17101394
- rs17101566
- rs17101659
- rs55676048
- rs55770157
- rs60045886
- rs61984086
- rs61984112
- rs72718380
- rs72718399
- rs72720338
- rs74056279
- rs74058330
- rs74659969
- rs75408790
- rs76229650
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.