Variant (rsID / SNP)
rs7522061
rs7522061 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FCRL3. Location: chromosome 1, position 157,668,390. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 1:157668390
- HGVS
- NM_001320333.2,c.82A>G,p.Asn28Asp
- Allele change
- Silent
Associated conditions / phenotypes
Autoimmune Disease|Allergic Rhinitis|Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity|Rhinitis|Sensorineural Hearing Loss|Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus|Sudden Sensorineural Hearing Loss|Inflammatory Spondylopathy|Spondyloarthropathy 1|Spondylitis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.