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Variant (rsID / SNP)

rs147215386

COL6A3

rs147215386 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL6A3. Location: chromosome 2, position 238,277,429. 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
2:238277429
Cytoband
2q37.3
HGVS
NM_004369.4(COL6A3):c.4677C>T (p.Phe1559=)
Allele change
Synonymous_F952F

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.