Variant (rsID / SNP)
rs112863054
rs112863054 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EVC2. Location: chromosome 4, position 5,617,337. Clinical significance in the table: Benign.
Reference-table entries
EVC2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:5617337
- Cytoband
- 4p16.2
- HGVS
- NM_147127.5(EVC2):c.2707-66C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.