RS75391579 GALT
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What This Variant Does
"rs75391579, also known as c.563A>
Associated Conditions
Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase
Galactosemia
Inborn genetic diseases
GALT-related disorder
Colorectal cancer
Malignant tumor of esophagus
Cervical cancer
Familial cancer of breast
Sarcoma
Melanoma
Thymoma
Acute myeloid leukemia
Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase
Galactosemia
Inborn genetic diseases
Other Variants in GALT