RS80356491 SLC37A4
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What This Variant Does
"rs80356491, also known as 1042_1043delCT or 1211-1212delCT, is a SNP in the solute carrier family 37...
Associated Conditions
Phosphate transport defect
Glucose-6-phosphate transport defect
Glycogen storage disease
Inborn genetic diseases
Congenital disorder of glycosylation
type IIw
type I
Phosphate transport defect
Glucose-6-phosphate transport defect
Glycogen storage disease
Inborn genetic diseases
Congenital disorder of glycosylation
type IIw
type I
Other Variants in SLC37A4