RS115198029 CRTAP

Health Risk Chr 3:33132670 snv missense variant

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Associated Conditions

Osteogenesis imperfecta type 7

Osteogenesis imperfecta

CRTAP-related disorder

Osteogenesis imperfecta type 7

Osteogenesis imperfecta

CRTAP-related disorder

Population Frequencies

gnomAD ALL

0.3%

1kG AFR

100%

1kG ALL

99.7%

1kG AMR

1.2%

1kG EAS

100%

1kG EUR

99.4%

1kG SAS

100%

Other Variants in CRTAP