Variant (rsID / SNP)
rs2231926
rs2231926 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EBLN2. Location: chromosome 3, position 73,111,809. The table records no clinical significance for this variant.
Reference-table entries
EBLN2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:73111809
- HGVS
- NM_018029.4,c.577A>G,p.Ile193Val
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.