Variant (rsID / SNP)
rs35692900
rs35692900 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCOLCE2. Location: chromosome 3, position 142,548,560. The table records no clinical significance for this variant.
Reference-table entries
PCOLCE2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:142548560
- HGVS
- NM_013363.4,c.839T>C,p.Val280Ala
- Allele change
- Missense_V280A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.