List of variants in gene TGFB1 reported as pathogenic by OMIM

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000660.7(TGFB1):c.1159T>C (p.Cys387Arg)	rs1336387628
NM_000660.7(TGFB1):c.652C>T (p.Arg218Cys)	rs104894721
NM_000660.7(TGFB1):c.653G>A (p.Arg218His)	rs104894720
NM_000660.7(TGFB1):c.667T>C (p.Cys223Arg)	rs104894722
NM_000660.7(TGFB1):c.667T>G (p.Cys223Gly)	rs104894722
NM_000660.7(TGFB1):c.673T>C (p.Cys225Arg)	rs104894719

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