RS119465999 UTP4

Health Risk Chr 16:69165385 snv missense variant

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What This Variant Does

"rs119465999, also known as c.1693C&gt

Associated Conditions

Hereditary North American Indian childhood cirrhosis

UTP4-related disorder

Hereditary North American Indian childhood cirrhosis

UTP4-related disorder

Population Frequencies

gnomAD ALL

99.9%

1kG AFR

100%

1kG ALL

0.2%

1kG AMR

98.8%

1kG EAS

100%

1kG EUR

0.1%

1kG SAS

100%

Other Variants in UTP4