Variant (rsID / SNP)
rs2076529
rs2076529 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BTNL2. Location: chromosome 6, position 32,363,955. The table records no clinical significance for this variant.
Reference-table entries
BTNL2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:32363955
- HGVS
- NM_001304561.2,c.939A>G,p.Val313Val
- Allele change
- Silent
Associated conditions / phenotypes
Non-Alcoholic Fatty Liver Disease|Liver Disease|Fatty Liver Disease|Sarcoidosis 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.