Variant (rsID / SNP)

rs121912938

rs121912938 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL6A1. Location: chromosome 21, position 47,409,043. Clinical significance in the table: Pathogenic.

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Reference-table entries

COL6A1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 21:47409043
Cytoband: 21q22.3
HGVS: NM_001848.3(COL6A1):c.850G>A (p.Gly284Arg)
Allele change: Missense_G284R

Associated conditions / phenotypes

Ullrich congenital muscular dystrophy 1, autosomal dominant|Bethlem myopathy 1|Ullrich congenital muscular dystrophy 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.