Variant (rsID / SNP)
rs55778272
rs55778272 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLXNA4. Location: chromosome 7, position 131,857,897. The table records no clinical significance for this variant.
Reference-table entries
PLXNA4Not classified
- Variant type
- intron_variant
- Chromosome / position
- 7:131857897
- HGVS
- NM_001393897.1,c.4017+1640A>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.