Variant (rsID / SNP)
rs7670299
rs7670299 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EVC2. Location: chromosome 4, position 5,576,140. Clinical significance in the table: Benign.
Reference-table entries
EVC2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:5576140
- Cytoband
- 4p16.2
- HGVS
- NM_147127.5(EVC2):c.3360+272A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.