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Variant (rsID / SNP)

rs137910388

COL6A3

rs137910388 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL6A3. Location: chromosome 2, position 238,305,427. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

COL6A3Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
2:238305427
Cytoband
2q37.3
HGVS
NM_004369.4(COL6A3):c.34G>A (p.Val12Ile)
Allele change
Missense_V12I

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.