RS141068211 ASAH1

Health Risk Chr 8:18062298
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Associated Conditions
Farber lipogranulomatosis
Self-limited epilepsy with centrotemporal spikes
Inborn genetic diseases
ASAH1-related disorders
Farber lipogranulomatosis
Self-limited epilepsy with centrotemporal spikes
Inborn genetic diseases
ASAH1-related disorders
Other Variants in ASAH1
rs137853593 rs137853594 rs137853595 rs137853596 rs137853597 rs145873635 rs397509415 rs794729663 rs200455852 rs756455049
Ask Dr. Hemsworth about this variant