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Variant (rsID / SNP)

rs114284669

COL6A3

rs114284669 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL6A3. Location: chromosome 2, position 238,285,445. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

COL6A3Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:238285445
Cytoband
2q37.3
HGVS
NM_004369.4(COL6A3):c.3040A>G (p.Lys1014Glu)
Allele change
Missense_K407E

Associated conditions / phenotypes

Bethlem myopathy 1|Ullrich congenital muscular dystrophy 1|Dystonia 27|Bethlem myopathy 1|Collagen 6-related myopathy

Public references

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