Gene entry
HSPA1L
heat shock protein family A (Hsp70) member 1 like
- Chromosome
- 6
- Cytoband
- 6p21.33
- Variants (rsID)
- 16
HSPA1L is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6p21.33). Its official name is “heat shock protein family A (Hsp70) member 1 like”. The reference table lists 16 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs139868987Associationsingle nucleotide variantInflammatory bowel disease 1
- rs34620296Associationsingle nucleotide variantInflammatory bowel disease 1
- rs2227955Benignsingle nucleotide variantInflammatory bowel disease 1
- rs2075799Not classifiedsynonymous_variantSchizophrenia|Systemic Lupus Erythematosus|Major Affective Disorder 8|Major Affective Disorder 9|Lupus Erythematosus|Bipolar Disorder
- rs2227956Not classifiedmissense_variantPulmonary Disease, Chronic Obstructive|Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus|Hearing Loss, Noise-Induced|Infertility|Male Infertility|Azoospermia|Spermatogenic Failure 50|Type 2 Diabetes Mellitus|Interstitial Lung Disease 2|Pulmonary Fibrosis|Lung Disease|Sensorineural Hearing Loss|Gastric Cancer|Schizophrenia|Multiple Sclerosis|Scrub Typhus|Epidemic Typhus|Pulmonary Edema
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.