Variant (rsID / SNP)
rs7302981
rs7302981 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CERS5. Location: chromosome 12, position 50,537,815. The table records no clinical significance for this variant.
Reference-table entries
CERS5Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:50537815
- HGVS
- NM_001331070.3,c.223T>C,p.Cys75Arg
- Allele change
- Silent
Associated conditions / phenotypes
Silent|Missense_C75R|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.