Gene entry
LOXHD1
lipoxygenase homology PLAT domains 1
- Chromosome
- 18
- Cytoband
- 18q21.1
- Variants (rsID)
- 85
LOXHD1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 18 (region 18q21.1). Its official name is “lipoxygenase homology PLAT domains 1”. The reference table lists 85 variants (rsID) for this gene.
Clinically classified variants
40 reference-table entries with clinical significance.
- rs10163657Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs12606417Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs142960762BenignMicrosatelliteAutosomal recessive nonsyndromic hearing loss 77
- rs188517529Benignsingle nucleotide variant
- rs34723936Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs7244681Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs112618498Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs113994614Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs114557260Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs115275492Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs116413527Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs118174674Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs143142227Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs146739496Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs146912450Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs148468627Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs16978578Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs182125538Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs187587197Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs188119157Conflicting interpretationssingle nucleotide variantRare genetic deafness|Autosomal recessive nonsyndromic hearing loss 77|Hearing impairment
- rs189873733Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs192376005Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs199645176Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs200068167Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs200518261Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs202043044Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs34589386Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs367826075Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs373924055Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs533251927Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs539688337Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs57330753Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs61733519Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs745683775Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77|Nonsyndromic genetic hearing loss
- rs78427072Likely benignsingle nucleotide variant
- rs121918370Pathogenicsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs201587138Pathogenicsingle nucleotide variantRare genetic deafness|Autosomal recessive nonsyndromic hearing loss 77|Nonsyndromic genetic hearing loss
- rs373937326Pathogenicsingle nucleotide variantRare genetic deafness|Autosomal recessive nonsyndromic hearing loss 77
- rs886044666Pathogenicsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
- rs182149228Uncertain significancesingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 77
Other listed variants
- rs101941
- rs328126
- rs328127
- rs328130
- rs328170
- rs328179
- rs328181
- rs328186
- rs674948
- rs732109
- rs1450428
- rs1450431
- rs1452277
- rs1462981
- rs1606889
- rs1979369
- rs4890331
- rs4890674
- rs7241561
- rs8093186
- rs9807265
- rs9946967
- rs11082547
- rs11665368
- rs11873154
- rs12604411
- rs12970992
- rs16939675
- rs34900262
- rs35940808
- rs72915418
- rs74384095
- rs74582486
- rs76345374
- rs80152962
- rs111331364
- rs111504720
- rs115528989
- rs116937573
- rs117013920
- rs117243386
- rs117318289
- rs117405702
- rs118148040
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.