Variant (rsID / SNP)

rs587779632

rs587779632 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL3A1. Location: chromosome 2, position 189,860,419. Clinical significance in the table: Pathogenic.

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Reference-table entries

COL3A1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 2:189860419
Cytoband: 2q32.2
HGVS: NM_000090.4(COL3A1):c.1511G>T (p.Gly504Val)
Allele change: Missense_G504V

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.