RS149026877 TMEM38B

Health Risk Chr 9:105774003
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Associated Conditions
Inborn genetic diseases
TMEM38B-related disorder
Osteogenesis imperfecta type 14
Inborn genetic diseases
TMEM38B-related disorder
Osteogenesis imperfecta type 14
Other Variants in TMEM38B
rs140157299 rs148378635 rs778527358 rs201882609 rs1179429999 rs201768590 rs199758976 rs1836361994 rs2540044767 rs376474086
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