List of variants in gene combination LOC126807519, TGFBI reported as uncertain significance for corneal disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000358.3(TGFBI):c.1127-11C>T	rs376923930	0.00021
NM_000358.3(TGFBI):c.1167C>T (p.Ser389=)	rs369100201	0.00002
NM_000358.3(TGFBI):c.1194C>T (p.Ala398=)	rs555953015	0.00002
NM_000358.3(TGFBI):c.1193C>A (p.Ala398Asp)	rs986231295

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