Gene entry
ROR2
ROR family WNT receptor 2
- Chromosome
- 9
- Cytoband
- 9q22.31
- Variants (rsID)
- 74
ROR2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q22.31). Its official name is “ROR family WNT receptor 2”. The reference table lists 74 variants (rsID) for this gene.
Clinically classified variants
17 reference-table entries with clinical significance.
- rs145568368Benignsingle nucleotide variantAutosomal recessive Robinow syndrome|Brachydactyly type B1
- rs188376581Benignsingle nucleotide variantBrachydactyly type B1|Autosomal recessive Robinow syndrome|Short stature
- rs34431454Benignsingle nucleotide variantBrachydactyly type B1|Autosomal recessive Robinow syndrome
- rs35852786Benignsingle nucleotide variantAutosomal recessive Robinow syndrome|Brachydactyly type B1
- rs41277837Benignsingle nucleotide variantAutosomal recessive Robinow syndrome|Brachydactyly type B1
- rs142386294Conflicting interpretationssingle nucleotide variantBrachydactyly type B1|Autosomal recessive Robinow syndrome
- rs144549032Conflicting interpretationssingle nucleotide variantAutosomal recessive Robinow syndrome|Brachydactyly type B1
- rs148237260Conflicting interpretationssingle nucleotide variantAutosomal recessive Robinow syndrome|Brachydactyly type B1
- rs149826387Conflicting interpretationssingle nucleotide variantBrachydactyly type B1|Autosomal recessive Robinow syndrome
- rs34491822Conflicting interpretationssingle nucleotide variantBrachydactyly, type B1Robinow syndrome, autosomal recessive|Brachydactyly type B1|Autosomal recessive Robinow syndrome
- rs34574788Conflicting interpretationssingle nucleotide variantBrachydactyly type B1|Autosomal recessive Robinow syndrome
- rs371221714Conflicting interpretationssingle nucleotide variantAutosomal recessive Robinow syndrome|Brachydactyly type B1
- rs41277835Conflicting interpretationssingle nucleotide variantAutosomal recessive Robinow syndrome|Brachydactyly type B1
- rs56099091Conflicting interpretationssingle nucleotide variantAutosomal recessive Robinow syndrome|Brachydactyly type B1
- rs56231927Conflicting interpretationssingle nucleotide variantAutosomal recessive Robinow syndrome|Brachydactyly type B1|Short stature
- rs121909087Pathogenicsingle nucleotide variantAutosomal recessive Robinow syndrome
- rs529829552Uncertain significancesingle nucleotide variantBrachydactyly, type B1Robinow syndrome, autosomal recessive|Autosomal recessive Robinow syndrome
Other listed variants
- rs1528363
- rs1892263
- rs2103301
- rs2872122
- rs3802377
- rs3824426
- rs3935382
- rs4067304
- rs4398991
- rs4467997
- rs7038823
- rs7041224
- rs7045073
- rs7863425
- rs7867961
- rs7875037
- rs9409651
- rs10739919
- rs10761133
- rs10992120
- rs10992121
- rs12002478
- rs12003273
- rs12340061
- rs12551140
- rs12552858
- rs16907798
- rs16907979
- rs17516460
- rs17586213
- rs56409414
- rs57980458
- rs62565753
- rs72744491
- rs73513284
- rs73651573
- rs73651595
- rs73651596
- rs75127805
- rs75153534
- rs76432051
- rs77019674
- rs77335334
- rs77618210
- rs111910246
- rs112309350
- rs114661477
- rs117005854
- rs117425435
- rs117703609
- rs117896627
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.