RS116099040 SPTBN2

Health Risk Chr 11:66705833 snv missense variant

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Associated Conditions

Inborn genetic diseases

SPTBN2-related disorder

Inborn genetic diseases

SPTBN2-related disorder

Population Frequencies

gnomAD ALL

100%

1kG AFR

99.8%

1kG ALL

99.9%

1kG AMR

99.9%

1kG EAS

100%

1kG EUR

100%

1kG SAS

100%

Other Variants in SPTBN2