RS587776752 TRAPPC2

Health Risk Chr X:13719866
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What This Variant Does
"CLNSIG=5
Associated Conditions
Spondyloepiphyseal dysplasia tarda
X-linked
Inborn genetic diseases
Spondyloepiphyseal dysplasia tarda
X-linked
Inborn genetic diseases
Other Variants in TRAPPC2
rs2146765756 rs2046281324 rs377210137 rs2046279070 rs2146776296 rs2146773091 rs2046258303 rs1312555296 rs2146775487 rs2518613150
Ask Dr. Hemsworth about this variant