List of variants in gene SMAD3 reported as uncertain significance for not specified

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_005902.4(SMAD3):c.207-26869C>A	rs958007552	0.00006
NM_005902.4(SMAD3):c.440C>T (p.Pro147Leu)	rs377026877	0.00005
NM_005902.4(SMAD3):c.872-12G>C	rs768529580	0.00004
NM_005902.4(SMAD3):c.1186A>G (p.Ile396Val)	rs1317532064	0.00003
NM_005902.4(SMAD3):c.632C>T (p.Pro211Leu)	rs772510704	0.00003
NM_005902.4(SMAD3):c.400+5G>T	rs766829176	0.00002
NM_005902.4(SMAD3):c.175A>G (p.Asn59Asp)	rs745387614	0.00001
NM_005902.4(SMAD3):c.532+8C>T	rs370879516	0.00001
NM_005902.4(SMAD3):c.1124G>T (p.Ser375Ile)
NM_005902.4(SMAD3):c.266G>A (p.Cys89Tyr)	rs1962535460
NM_005902.4(SMAD3):c.269G>A (p.Arg90His)	rs886038803
NM_005902.4(SMAD3):c.727C>T (p.Arg243Cys)	rs886039137
NM_005902.4(SMAD3):c.850G>C (p.Glu284Gln)	rs886038991
NM_005902.4(SMAD3):c.908T>A (p.Val303Asp)	rs1555414011
NM_005902.4(SMAD3):c.967C>T (p.Arg323Cys)	rs967072552

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