Gene entry
NEBL
nebulette
- Chromosome
- 10
- Cytoband
- 10p12.31
- Variants (rsID)
- 126
NEBL is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10p12.31). Its official name is “nebulette”. The reference table lists 126 variants (rsID) for this gene.
Clinically classified variants
18 reference-table entries with clinical significance.
- rs2296610Benignsingle nucleotide variantPrimary dilated cardiomyopathy|Cardiovascular phenotype
- rs41277370Benignsingle nucleotide variantCardiovascular phenotype|Primary dilated cardiomyopathy
- rs71578975Benignsingle nucleotide variantPrimary dilated cardiomyopathy|Cardiovascular phenotype
- rs114875104Conflicting interpretationssingle nucleotide variantPrimary dilated cardiomyopathy
- rs137973321Conflicting interpretationssingle nucleotide variantPrimary dilated cardiomyopathy
- rs139610204Conflicting interpretationssingle nucleotide variantPrimary dilated cardiomyopathy
- rs139809958Conflicting interpretationssingle nucleotide variantPrimary dilated cardiomyopathy
- rs146275785Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Primary dilated cardiomyopathy
- rs193163659Conflicting interpretationssingle nucleotide variantPrimary dilated cardiomyopathy
- rs201822024Conflicting interpretationssingle nucleotide variantPrimary dilated cardiomyopathy
- rs368268112Conflicting interpretationssingle nucleotide variantPrimary dilated cardiomyopathy|Cardiovascular phenotype
- rs41277374Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Primary dilated cardiomyopathy
- rs578252294Conflicting interpretationssingle nucleotide variantPrimary dilated cardiomyopathy
- rs75301590Conflicting interpretationssingle nucleotide variantPrimary dilated cardiomyopathy
- rs780384504Conflicting interpretationssingle nucleotide variantPrimary dilated cardiomyopathy|Cardiovascular phenotype
- rs143584663Likely benignsingle nucleotide variantPrimary dilated cardiomyopathy
- rs151035799Likely benignsingle nucleotide variantPrimary dilated cardiomyopathy
- rs151012132Uncertain significancesingle nucleotide variantPrimary dilated cardiomyopathy
Other listed variants
- rs11995
- rs478559
- rs526061
- rs561415
- rs621429
- rs640056
- rs660859
- rs663661
- rs703088
- rs788963
- rs788965
- rs788970
- rs946861
- rs952738
- rs971015
- rs974255
- rs1417184
- rs1832677
- rs1841530
- rs1979486
- rs2119243
- rs2279311
- rs3802729
- rs3802730
- rs3847375
- rs3858199
- rs3900782
- rs4575164
- rs4631770
- rs4748752
- rs7083342
- rs7085330
- rs7085480
- rs7086221
- rs7090013
- rs7090954
- rs7095405
- rs7099403
- rs7896069
- rs7896127
- rs7898090
- rs7904221
- rs7913231
- rs7915437
- rs7916026
- rs9663304
- rs9665295
- rs10508634
- rs10764307
- rs10828151
- rs10828176
- rs10828212
- rs10828230
- rs11012340
- rs11012365
- rs11012416
- rs11012417
- rs11012503
- rs11012506
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.