Gene entry
LRMDA
leucine rich melanocyte differentiation associated
- Chromosome
- 10
- Cytoband
- 10q22.2-q22.3
- Variants (rsID)
- 353
LRMDA is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q22.2-q22.3). Its official name is “leucine rich melanocyte differentiation associated”. The reference table lists 353 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs1898071Benignsingle nucleotide variantOculocutaneous albinism type 7
- rs35349706Benignsingle nucleotide variant
- rs75852090Benignsingle nucleotide variant
- rs146123023Conflicting interpretationsDeletion
Other listed variants
- rs749128
- rs877531
- rs942091
- rs960174
- rs1040936
- rs1124372
- rs1247479
- rs1247488
- rs1323072
- rs1323074
- rs1367290
- rs1430331
- rs1865632
- rs1873468
- rs1885822
- rs1898072
- rs1898089
- rs1898098
- rs1907302
- rs1907341
- rs1907345
- rs1907348
- rs1946709
- rs2057435
- rs2057440
- rs2208948
- rs2395289
- rs2573559
- rs2579790
- rs2637256
- rs2758964
- rs2894318
- rs4745785
- rs4745804
- rs4745816
- rs4746337
- rs4746346
- rs4746363
- rs4746393
- rs6480804
- rs7077442
- rs7082211
- rs7086089
- rs7087207
- rs7087208
- rs7090265
- rs7093663
- rs7097617
- rs7895997
- rs7896671
- rs7899456
- rs7900522
- rs7901344
- rs7909650
- rs7910498
- rs7920628
- rs9415126
- rs9415127
- rs9415128
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.