RS11581921 P3H1

Health Risk Chr 1:42750258 snv missense variant

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Associated Conditions

Osteogenesis imperfecta type 8

Osteogenesis Imperfecta

Recessive

Osteogenesis imperfecta type 8

Osteogenesis Imperfecta

Recessive

Population Frequencies

gnomAD ALL

92.2%

1kG AFR

98.9%

1kG ALL

94.2%

1kG AMR

95%

1kG EAS

95.9%

1kG EUR

91.6%

1kG SAS

88.4%

Other Variants in P3H1