RS121908532 SLC25A13

Health Risk Chr 7:96121733
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What This Variant Does
"SLC25A13 gene, c.1763G&gt
Associated Conditions
Citrullinemia type II
Inborn genetic diseases
Citrullinemia
Neonatal intrahepatic cholestasis due to citrin deficiency
Citrin deficiency
Citrullinemia type II
Inborn genetic diseases
Citrullinemia
Neonatal intrahepatic cholestasis due to citrin deficiency
Citrin deficiency
Other Variants in SLC25A13
rs80338722 rs80338725 rs80338719 rs80338723 rs80338726 rs80338721 rs80338724 rs80338715 rs80338727 rs80338729
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