Variant (rsID / SNP)
rs9555703
rs9555703 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL4A2. Location: chromosome 13, position 111,109,882. The table records no clinical significance for this variant.
Reference-table entries
COL4A2Not classified
- Variant type
- intron_variant
- Chromosome / position
- 13:111109882
- HGVS
- NM_001846.4,c.1432+100A>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.