List of variants in gene GRHL2 reported as benign for corneal dystrophy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_024915.4(GRHL2):c.-24C>G	rs515622	0.98894
NM_024915.4(GRHL2):c.*41G>A	rs3735713	0.37317
NM_024915.4(GRHL2):c.1764-19C>T	rs10093032	0.37291

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