Gene entry
NHS
NHS actin remodeling regulator
- Chromosome
- X
- Cytoband
- Xp22.2-p22.13
- Variants (rsID)
- 57
NHS is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp22.2-p22.13). Its official name is “NHS actin remodeling regulator”. The reference table lists 57 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs140904281Benignsingle nucleotide variantHistory of neurodevelopmental disorder|Nance-Horan syndrome
- rs149244552Benignsingle nucleotide variantHistory of neurodevelopmental disorder|Nance-Horan syndrome
- rs150688899Benignsingle nucleotide variantNance-Horan syndrome|History of neurodevelopmental disorder
- rs3747295Benignsingle nucleotide variantHistory of neurodevelopmental disorder|Nance-Horan syndrome
- rs41304731Benignsingle nucleotide variantNance-Horan syndrome
- rs145005596Conflicting interpretationssingle nucleotide variantHistory of neurodevelopmental disorder|Nance-Horan syndrome
- rs132630322Pathogenicsingle nucleotide variantNance-Horan syndrome
- rs372969054Uncertain significancesingle nucleotide variantInborn genetic diseases
Other listed variants
- rs916313
- rs1007420
- rs1883665
- rs2071849
- rs4134188
- rs4825256
- rs4825269
- rs4825303
- rs4825330
- rs4825335
- rs4825340
- rs4825352
- rs4825360
- rs4825363
- rs5909373
- rs5909374
- rs5955543
- rs5955731
- rs6418708
- rs6629232
- rs6632976
- rs6632979
- rs9887234
- rs10856285
- rs11798583
- rs12010218
- rs12013261
- rs12392758
- rs16980618
- rs16980636
- rs16980652
- rs16980660
- rs17246582
- rs17312492
- rs34577291
- rs55703216
- rs58684845
- rs66502455
- rs78153843
- rs79955925
- rs116551633
- rs138640416
- rs138975293
- rs181693134
- rs184526597
- rs189281793
- rs190617879
- rs200313691
- rs201092111
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.