Variant (rsID / SNP)

rs587779591

rs587779591 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL3A1. Location: chromosome 2, position 189,864,075. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

COL3A1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 2:189864075
Cytoband: 2q32.2
HGVS: NM_000090.4(COL3A1):c.2087G>A (p.Gly696Asp)
Allele change: Missense_G696D

Associated conditions / phenotypes

Ehlers-Danlos syndrome, type 4

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.