Gene entry
LPIN1
lipin 1
- Chromosome
- 2
- Cytoband
- 2p25.1
- Variants (rsID)
- 51
LPIN1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p25.1). Its official name is “lipin 1”. The reference table lists 51 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs10182021Benignsingle nucleotide variant
- rs13392363Benignsingle nucleotide variant
- rs33997857Benignsingle nucleotide variantMyoglobinuria, acute recurrent, autosomal recessive
- rs3795974Benignsingle nucleotide variant
- rs4669781Benignsingle nucleotide variantMyoglobinuria, acute recurrent, autosomal recessive
Other listed variants
- rs4076903
- rs4296403
- rs4471859
- rs4669776
- rs4669780
- rs6721977
- rs6729430
- rs6755975
- rs7572205
- rs7580386
- rs10191977
- rs10192566
- rs10495584
- rs11691729
- rs11693935
- rs11695025
- rs11889885
- rs12616402
- rs13412852
- rs17603350
- rs17603420
- rs34857485
- rs59246568
- rs60181205
- rs72493341
- rs72773985
- rs73179398
- rs73181372
- rs73189031
- rs73189040
- rs75383321
- rs75618981
- rs79828866
- rs80226034
- rs114935785
- rs115050984
- rs115240286
- rs116203369
- rs116420413
- rs117689008
- rs181987568
- rs182735664
- rs190743128
- rs192272279
- rs193081606
- rs201940484
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.