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Variant (rsID / SNP)

rs760649238

COL6A1

rs760649238 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL6A1. Location: chromosome 21, position 47,422,174. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

COL6A1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
21:47422174
Cytoband
21q22.3
HGVS
NM_001848.3(COL6A1):c.2109G>A (p.Thr703=)
Allele change
Synonymous_T703T

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.