RS41297065 SLC46A1

Health Risk Chr 17:28406093
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Associated Conditions
Congenital defect of folate absorption
SLC46A1-related disorder
Inborn genetic diseases
Congenital defect of folate absorption
SLC46A1-related disorder
Inborn genetic diseases
Other Variants in SLC46A1
rs80338775 rs80338769 rs80338770 rs80338772 rs80338773 rs80338774 rs397515574 rs281875208 rs397515391 rs281875209
Ask Dr. Hemsworth about this variant