RS137885421 FLNB

Health Risk Chr 3:58148807 snv missense variant

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Associated Conditions

FLNB-Related Spectrum Disorders

Inborn genetic diseases

FLNB-related disorder

FLNB-Related Spectrum Disorders

Inborn genetic diseases

FLNB-related disorder

Population Frequencies

gnomAD ALL

100%

1kG AFR

99.7%

1kG ALL

99.9%

1kG AMR

100%

1kG EAS

100%

1kG EUR

100%

1kG SAS

100%

Other Variants in FLNB