RS80338775 SLC46A1

Health Risk Chr 17:28402322
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What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital defect of folate absorption
Inborn genetic diseases
SLC46A1-related disorder
Congenital defect of folate absorption
Inborn genetic diseases
SLC46A1-related disorder
Other Variants in SLC46A1
rs80338769 rs80338770 rs80338772 rs80338773 rs80338774 rs397515574 rs281875208 rs397515391 rs281875209 rs281875211
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