RS80338770 SLC46A1
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What This Variant Does
"Congenital folate malabsorption. The spectrum of mutations in the PCFT gene, coding for an intestina...
Associated Conditions
Congenital defect of folate absorption
Congenital defect of folate absorption
Congenital defect of folate absorption
Congenital defect of folate absorption
Other Variants in SLC46A1