List of variants reported as uncertain significance for Gastrointestinal defects and immunodeficiency syndrome 1 by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_020458.4(TTC7A):c.974G>A (p.Arg325Gln)	rs144971707	0.00055
NM_020458.4(TTC7A):c.794G>A (p.Arg265Gln)	rs78745374	0.00015
NM_020458.4(TTC7A):c.1616C>T (p.Ser539Leu)	rs776906926	0.00001
NM_020458.4(TTC7A):c.436C>T (p.Arg146Trp)	rs138592761	0.00001

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