Variant (rsID / SNP)

rs201220788

rs201220788 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL3A1. Location: chromosome 2, position 189,870,163. Clinical significance in the table: Likely benign.

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Reference-table entries

COL3A1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:189870163
Cytoband: 2q32.2
HGVS: NM_000090.4(COL3A1):c.3019G>A (p.Ala1007Thr)
Allele change: Missense_A1007T

Associated conditions / phenotypes

Cardiovascular phenotype|Ehlers-Danlos syndrome, type 4|Familial thoracic aortic aneurysm and aortic dissection

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.