RS121434480 HPGD

Health Risk Chr 4:174508699
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What This Variant Does
"[OMIM:?]
Associated Conditions
Cranioosteoarthropathy
Hypertrophic osteoarthropathy
primary
autosomal recessive
1
Cranioosteoarthropathy
Hypertrophic osteoarthropathy
primary
autosomal recessive
1
Other Variants in HPGD
rs751774080 rs747458590 rs1579268244 rs2477896212 rs2477966287 rs1735312842 rs769423339 rs1166031576 rs2477840776 rs1191997234
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