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Variant (rsID / SNP)

rs184617787

COL6A3

rs184617787 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL6A3. Location: chromosome 2, position 238,233,467. 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
2:238233467
Cytoband
2q37.3
HGVS
NM_004369.4(COL6A3):c.9494-10C>T
Allele change
Silent

Associated conditions / phenotypes

Collagen 6-related myopathy|Bethlem myopathy 1

Public references

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