RS397515391 SLC46A1

Health Risk Chr 17:28405910
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What This Variant Does
"CLNSIG=5
Associated Conditions
Congenital defect of folate absorption
Congenital defect of folate absorption
Other Variants in SLC46A1
rs80338775 rs80338769 rs80338770 rs80338772 rs80338773 rs80338774 rs397515574 rs281875208 rs281875209 rs281875211
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