"GRHL2-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2635445	NM_024915.4(GRHL2):c.21-1G>A	GRHL2	Single nucleotide variant (splice acceptor variant)	GRHL2-related condition	GLikely pathogenic
Select item 163646	NM_024915.4(GRHL2):c.543G>A (p.Glu181=)	GRHL2	Single nucleotide variant (synonymous variant)	GRHL2-related condition +2 more	GLikely benign
Select item 227418	NM_024915.4(GRHL2):c.816A>G (p.Lys272=)	GRHL2	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 1201866	NM_024915.4(GRHL2):c.1245C>T (p.Val415=)	GRHL2	Single nucleotide variant (synonymous variant)	GRHL2-related condition +1 more	GLikely benign
Select item 3030376	NM_024915.4(GRHL2):c.1335A>G (p.Gln445=)	GRHL2	Single nucleotide variant (synonymous variant)	GRHL2-related condition	GLikely benign
Select item 1961457	NM_024915.4(GRHL2):c.1610G>A (p.Arg537Gln)	LOC126860461, GRHL2 (R521Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 730309	NM_024915.4(GRHL2):c.1698+7C>T	GRHL2	Single nucleotide variant (intron variant)	GRHL2-related condition +1 more	GLikely benign

ClinVar