List of variants reported as likely benign for Congenital defect of folate absorption by Illumina Laboratory Services, Illumina

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_080669.6(SLC46A1):c.*4316C>G	rs117397871	0.01065
NM_080669.6(SLC46A1):c.*2123G>C	rs7225850	0.00854
NM_080669.6(SLC46A1):c.*3120A>G	rs147971222	0.00348
NM_080669.6(SLC46A1):c.*1648G>A	rs114008979	0.00295
NM_080669.6(SLC46A1):c.756C>G (p.Val252=)	rs185900287	0.00274
NM_080669.6(SLC46A1):c.*2852C>T	rs569526091	0.00243
NM_080669.6(SLC46A1):c.642G>A (p.Leu214=)	rs145398587	0.00145
NM_080669.6(SLC46A1):c.294C>A (p.Leu98=)	rs371270310	0.00110
NM_080669.6(SLC46A1):c.*1332G>A	rs146041886	0.00101
NM_080669.6(SLC46A1):c.*1392C>A	rs141940033	0.00011
NM_080669.6(SLC46A1):c.*60G>T	rs41297121	0.00006
NM_080669.6(SLC46A1):c.*4035G>A	rs569679076
NM_080669.6(SLC46A1):c.906A>G (p.Lys302=)	rs572650603

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