Gene entry
FHL2
four and a half LIM domains 2
- Chromosome
- 2
- Cytoband
- 2q12.2
- Variants (rsID)
- 37
FHL2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q12.2). Its official name is “four and a half LIM domains 2”. The reference table lists 37 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs56284940Benignsingle nucleotide variantPrimary dilated cardiomyopathy|Cardiomyopathy
- rs200116659Uncertain significancesingle nucleotide variantPrimary dilated cardiomyopathy
Other listed variants
- rs880427
- rs1914748
- rs2278501
- rs6737809
- rs6750100
- rs6753046
- rs7597058
- rs7599750
- rs10169988
- rs10190186
- rs10194273
- rs11124031
- rs11676660
- rs11690543
- rs11694681
- rs11893160
- rs12475649
- rs12614625
- rs17030823
- rs34478379
- rs55756009
- rs57573753
- rs60670857
- rs62152123
- rs72836940
- rs72945042
- rs76181834
- rs77770844
- rs80218684
- rs114952738
- rs115452935
- rs115701464
- rs116213921
- rs117871643
- rs149107151
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
