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Variant (rsID / SNP)

rs368800027

COL6A3

rs368800027 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL6A3. Location: chromosome 2, position 238,296,391. 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
2:238296391
Cytoband
2q37.3
HGVS
NM_004369.4(COL6A3):c.1146G>A (p.Gln382=)
Allele change
Silent

Associated conditions / phenotypes

Bethlem myopathy 1

Public references

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