RS121912885 COL2A1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Stickler syndrome
type I
nonsyndromic ocular
Stickler syndrome type 1
Inborn genetic diseases
Stickler syndrome
type I
nonsyndromic ocular
Stickler syndrome type 1
Inborn genetic diseases
Other Variants in COL2A1