List of variants in gene TGFBI reported as likely pathogenic 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000358.3(TGFBI):c.1406G>A (p.Arg469His)	rs376761086	0.00002
NM_000358.3(TGFBI):c.1501C>A (p.Pro501Thr)	rs121909212
NM_000358.3(TGFBI):c.1517_1518insCAAGGG (p.Met506delinsIleLysGly)
NM_000358.3(TGFBI):c.1612A>C (p.Thr538Pro)	rs2126915354
NM_000358.3(TGFBI):c.1772C>A (p.Ser591Tyr)	rs1751703312
NM_000358.3(TGFBI):c.1855A>G (p.Met619Val)	rs2126917684
NM_000358.3(TGFBI):c.1864A>C (p.Asn622His)	rs2126917690

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