C3463897[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1588	NM_001127255.2(NLRP7):c.2738A>G (p.Asn913Ser)	NCR1, NLRP7 (N913S +1 more)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1	GLikely pathogenic
Select item 894311	NM_001127255.2(NLRP7):c.467G>A (p.Arg156Gln)	NLRP7 (R156Q)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1 +1 more	GBenign/Likely benign