C4747961[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 178378	NM_024915.4(GRHL2):c.548G>A (p.Arg183Gln)	GRHL2 (R183Q +1 more)	Single nucleotide variant (missense variant)	not specified +4 more	GUncertain significance
Select item 46214	NM_024915.4(GRHL2):c.1098+9C>T	GRHL2	Single nucleotide variant (intron variant)	Corneal dystrophy, posterior polymorphous, 4 +4 more	GBenign/Likely benign
Select item 46216	NM_024915.4(GRHL2):c.1723G>A (p.Val575Met)	GRHL2 (V575M +1 more)	Single nucleotide variant (missense variant)	not specified +5 more	GUncertain significance

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