Variant (rsID / SNP)
rs2778979
rs2778979 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLXDC2. Location: chromosome 10, position 20,534,333. The table records no clinical significance for this variant.
Reference-table entries
PLXDC2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:20534333
- HGVS
- NM_032812.9,c.1372A>G,p.Ile458Val
- Allele change
- Missense_I409V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.