RS118049905 UNC13D

Health Risk Chr 17:75830085 snv missense variant

Upload your DNA to see your genotype for this variant.

Associated Conditions

Familial hemophagocytic lymphohistiocytosis 3

Autoinflammatory syndrome

Familial hemophagocytic lymphohistiocytosis 3

Autoinflammatory syndrome

Population Frequencies

gnomAD ALL

99.4%

1kG AFR

100%

1kG ALL

99.8%

1kG AMR

99.6%

1kG EAS

100%

1kG EUR

0.6%

1kG SAS

100%

Other Variants in UNC13D