List of variants in gene TGFB1 reported as uncertain significance for bone disorder

Minimum submission review status:		Collection method:
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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_000660.7(TGFB1):c.32T>A (p.Leu11Gln)	rs867906741	0.00003
NM_000660.7(TGFB1):c.535T>C (p.Trp179Arg)	rs1568478752
NM_000660.7(TGFB1):c.712G>A (p.Gly238Arg)	rs1454205854

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