Variant (rsID / SNP)
rs1594
rs1594 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFLAR. Location: chromosome 2, position 202,025,621. The table records no clinical significance for this variant.
Reference-table entries
CFLARNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 2:202025621
- HGVS
- NM_001127183.4,c.1260A>G,p.Pro420Pro
- Allele change
- Silent
Associated conditions / phenotypes
Synonymous_P420P|Silent|Synonymous_P420P|Silent|Synonymous_P324P|Synonymous_P324P|Silent|Synonymous_P420P|Synonymous_P420P|Synonymous_P324P|Synonymous_P175P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.