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Variant (rsID / SNP)

rs146789395

COL5A2

rs146789395 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL5A2. Location: chromosome 2, position 189,909,952. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

COL5A2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:189909952
Cytoband
2q32.2
HGVS
NM_000393.5(COL5A2):c.3316C>T (p.Arg1106Trp)
Allele change
Missense_R1106W

Associated conditions / phenotypes

Ehlers-Danlos syndrome type 7A|Ehlers-Danlos syndrome, classic type, 1|Connective tissue disorder|Cardiovascular phenotype|Ehlers-Danlos syndrome, classic type, 2

Public references

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