List of variants in gene TGFBI reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000358.3(TGFBI):c.1620T>C (p.Phe540=)	rs4669	0.38557
NM_000358.3(TGFBI):c.651G>C (p.Leu217=)	rs1442	0.36069
NM_000358.3(TGFBI):c.981A>G (p.Val327=)	rs1054124	0.35276
NM_000358.3(TGFBI):c.1416C>T (p.Leu472=)	rs1133170	0.27861
NM_000358.3(TGFBI):c.460-16C>T	rs41298960	0.04646
NM_000358.3(TGFBI):c.1749C>T (p.Ile583=)	rs35909506	0.00104
NM_000358.3(TGFBI):c.805C>T (p.Leu269Phe)	rs199852470	0.00058
NM_000358.3(TGFBI):c.969G>A (p.Ala323=)	rs533421485	0.00001
NM_000358.3(TGFBI):c.1584G>A (p.Thr528=)	rs552261238
NM_000358.3(TGFBI):c.1950G>A (p.Ala650=)
NM_000358.3(TGFBI):c.50G>C (p.Gly17Ala)
NM_000358.3(TGFBI):c.690C>T (p.His230=)

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