RS104893637 MATN3
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Multiple epiphyseal dysplasia type 5
Multiple epiphyseal dysplasia
Spondyloepimetaphyseal dysplasia
matrilin-3 type
Inborn genetic diseases
Multiple epiphyseal dysplasia type 5
Multiple epiphyseal dysplasia
Spondyloepimetaphyseal dysplasia
matrilin-3 type
Inborn genetic diseases
Other Variants in MATN3