List of variants reported as likely pathogenic for malabsorption syndrome by Baylor Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001041.4(SI):c.3218G>A (p.Gly1073Asp)	rs121912616	0.00150
NM_001041.4(SI):c.1730T>G (p.Val577Gly)	rs121912615	0.00131
NM_014009.4(FOXP3):c.315+1G>A
NM_014009.4(FOXP3):c.970T>C (p.Phe324Leu)	rs122467173

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