RS863223288 TNFSF11

Health Risk Chr 13:42606792
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive osteopetrosis 2
Autosomal recessive osteopetrosis 2
Other Variants in TNFSF11
rs2137905441 rs121909072 rs267603829 rs142756983 rs151215329 rs146484645 rs200250962 rs189501562 rs775866494 rs746313384
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