List of variants in gene TGFBR1 reported as pathogenic for not provided

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004612.4(TGFBR1):c.1460G>A (p.Arg487Gln)	rs113605875	0.00001
GRCh37/hg19 9q22.33(chr9:101878960-101949121)x1
NM_004612.4(TGFBR1):c.1126A>G (p.Lys376Glu)	rs2118807458
NM_004612.4(TGFBR1):c.1459C>T (p.Arg487Trp)	rs111426349
NM_004612.4(TGFBR1):c.680AAG[1] (p.Glu228del)	rs863223829
NM_004612.4(TGFBR1):c.722C>T (p.Ser241Leu)	rs111854391
NM_004612.4(TGFBR1):c.797A>G (p.Asp266Gly)	rs863223819

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