Variant (rsID / SNP)

rs17357592

rs17357592 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL6A2. Location: chromosome 21, position 47,542,779. Clinical significance in the table: Benign.

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Reference-table entries

COL6A2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 21:47542779
Cytoband: 21q22.3
HGVS: NM_001849.4(COL6A2):c.1609-10C>T
Allele change: Silent

Associated conditions / phenotypes

Myosclerosis|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.