Gene entry
LAMA5
laminin subunit alpha 5
- Chromosome
- 20
- Cytoband
- 20q13.33
- Variants (rsID)
- 46
LAMA5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20q13.33). Its official name is “laminin subunit alpha 5”. The reference table lists 46 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
Other listed variants
- rs512452
- rs875379
- rs1741640
- rs2427293
- rs4925386
- rs13039398
- rs34000043
- rs41307203
- rs45496002
- rs62204553
- rs74425823
- rs74906764
- rs77172131
- rs77713982
- rs79319629
- rs80097864
- rs112963711
- rs116895933
- rs116912780
- rs117495689
- rs138514452
- rs138627467
- rs139973497
- rs141208202
- rs141989486
- rs142571210
- rs144009130
- rs144289855
- rs148177752
- rs149169462
- rs149358620
- rs150196385
- rs189209648
- rs190143217
- rs199655569
- rs199704088
- rs200037423
- rs200132013
- rs200148340
- rs201130283
- rs202214661
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
