Variant (rsID / SNP)

rs146662894

rs146662894 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL6A1. Location: chromosome 21, position 47,423,309. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

COL6A1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 21:47423309
Cytoband: 21q22.3
HGVS: NM_001848.3(COL6A1):c.2469G>A (p.Thr823=)
Allele change: Synonymous_T823T

Associated conditions / phenotypes

Collagen 6-related myopathy|Bethlem myopathy 1

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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