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Variant (rsID / SNP)

rs141593495

COL12A1

rs141593495 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL12A1. Location: chromosome 6, position 75,828,890. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

COL12A1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
6:75828890
Cytoband
6q13
HGVS
NM_004370.6(COL12A1):c.7223C>T (p.Thr2408Met)
Allele change
Missense_T1244M

Associated conditions / phenotypes

Ullrich congenital muscular dystrophy 2|Bethlem myopathy 2

Public references

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