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Variant (rsID / SNP)

rs61736966

COL5A1

rs61736966 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL5A1. Location: chromosome 9, position 137,688,701. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

COL5A1Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
9:137688701
Cytoband
9q34.3
HGVS
NM_000093.5(COL5A1):c.2852A>G (p.Asn951Ser)
Allele change
Missense_N951S

Associated conditions / phenotypes

Ehlers-Danlos syndrome type 7A|Cardiovascular phenotype|Ehlers-Danlos syndrome, classic type, 1|Ehlers-Danlos syndrome|FIBROMUSCULAR DYSPLASIA, MULTIFOCAL

Public references

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