RS201837257 SLC46A1

Health Risk Chr 17:28405074
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Associated Conditions
Congenital defect of folate absorption
Intellectual disability
Inborn genetic diseases
Congenital defect of folate absorption
Intellectual disability
Inborn genetic diseases
Other Variants in SLC46A1
rs80338775 rs80338769 rs80338770 rs80338772 rs80338773 rs80338774 rs397515574 rs281875208 rs397515391 rs281875209
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