RS776813259 SLCO2A1

Health Risk Chr 3:133935781
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hypertrophic osteoarthropathy
primary
autosomal recessive
2
autosomal dominant
Hypertrophic osteoarthropathy
primary
autosomal recessive
2
autosomal dominant
Other Variants in SLCO2A1
rs1559943990 rs387906806 rs1559927542 rs751192029 rs370769816 rs387907295 rs387907296 rs387907297 rs1085307096 rs765249238
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