RS114895145 HRG

Health Risk Chr 3:186666155 snv missense variant

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Associated Conditions

Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency

Thrombus

HRG-related disorder

Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency

Thrombus

HRG-related disorder

Population Frequencies

gnomAD ALL

1kG AFR

0.3%

1kG ALL

99.8%

1kG AMR

0.3%

1kG EAS

100%

1kG EUR

0.4%

1kG SAS

100%

Other Variants in HRG