List of variants reported as pathogenic for pregnancy disorder by Fulgent Genetics, Fulgent Genetics

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000369.5(TSHR):c.1349G>A (p.Arg450His)	rs189261858	0.00023
NM_000369.5(TSHR):c.1637G>A (p.Trp546Ter)	rs121908866	0.00021
NM_000103.4(CYP19A1):c.628G>A (p.Glu210Lys)	rs121434538	0.00001
NM_000369.5(TSHR):c.1657G>A (p.Ala553Thr)	rs121908872
NM_000901.5(NR3C2):c.1951C>T (p.Arg651Ter)	rs1131691921
NM_000901.5(NR3C2):c.1954C>T (p.Arg652Ter)
NM_000901.5(NR3C2):c.2839C>T (p.Arg947Ter)	rs121912569

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