Gene entry
LAMA4
laminin subunit alpha 4
- Chromosome
- 6
- Cytoband
- 6q21
- Variants (rsID)
- 54
LAMA4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6q21). Its official name is “laminin subunit alpha 4”. The reference table lists 54 variants (rsID) for this gene.
Clinically classified variants
22 reference-table entries with clinical significance.
- rs11757455Benignsingle nucleotide variantDilated cardiomyopathy 1JJ
- rs2032567Benignsingle nucleotide variantDilated cardiomyopathy 1JJ
- rs35349917Benignsingle nucleotide variantDilated cardiomyopathy 1JJ|Cardiomyopathy
- rs35605307Benignsingle nucleotide variantCardiovascular phenotype|Dilated cardiomyopathy 1JJ|Primary dilated cardiomyopathy
- rs3734292Benignsingle nucleotide variantDilated cardiomyopathy 1JJ|Cardiomyopathy
- rs41289902Benignsingle nucleotide variantDilated cardiomyopathy 1JJ|Cardiomyopathy
- rs6917763Benignsingle nucleotide variantDilated cardiomyopathy 1JJ
- rs141988342Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1JJ|Cardiovascular phenotype|Cardiomyopathy
- rs143269044Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1JJ|Cardiovascular phenotype|Cardiomyopathy|Arrhythmogenic right ventricular cardiomyopathy
- rs146868519Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1JJ|Cardiovascular phenotype|Cardiomyopathy|Primary dilated cardiomyopathy
- rs150069819Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Dilated cardiomyopathy 1JJ
- rs150084275Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1JJ
- rs183262122Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1JJ|Cardiovascular phenotype|Cardiomyopathy
- rs200112094Conflicting interpretationssingle nucleotide variantPrimary familial hypertrophic cardiomyopathy|Dilated cardiomyopathy 1JJ
- rs200177134Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1JJ
- rs201209516Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1JJ
- rs373650093Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Cardiomyopathy|Dilated cardiomyopathy 1JJ|Premature ventricular contraction
- rs3752579Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Hypertrophic cardiomyopathy|Cardiomyopathy|Dilated cardiomyopathy 1JJ
- rs70940811Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Dilated cardiomyopathy 1JJ|Cardiomyopathy
- rs73532636Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Dilated cardiomyopathy 1JJ
- rs147695488Likely benignsingle nucleotide variantCardiovascular phenotype|Dilated cardiomyopathy 1JJ
- rs181787647Uncertain significancesingle nucleotide variantDilated cardiomyopathy 1JJ
Other listed variants
- rs764587
- rs971402
- rs2072022
- rs2213840
- rs2237243
- rs2237244
- rs2237246
- rs3798357
- rs6904691
- rs6926573
- rs9398302
- rs9487853
- rs12204892
- rs12210552
- rs12214148
- rs34072237
- rs34172193
- rs76951179
- rs77165496
- rs77199140
- rs77886563
- rs112041077
- rs113109272
- rs117141652
- rs117617193
- rs117675557
- rs117827295
- rs142156703
- rs191973184
- rs200238782
- rs201094782
- rs201834379
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.