Variant (rsID / SNP)
rs2287803
rs2287803 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL5A3. Location: chromosome 19, position 10,112,346. The table records no clinical significance for this variant.
Reference-table entries
COL5A3Not classified
- Variant type
- missense_variant&splice_region_variant
- Chromosome / position
- 19:10112346
- HGVS
- NM_015719.4,c.964A>G,p.Arg322Gly
- Allele change
- Missense_R322G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.