List of variants in gene SMAD3 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_005902.4(SMAD3):c.885G>A (p.Arg295=)	rs139616052	0.00009
NM_005902.4(SMAD3):c.1258C>T (p.Arg420Cys)	rs1206533102	0.00003
NM_005902.4(SMAD3):c.334G>A (p.Ala112Thr)	rs770798158	0.00002
NM_005902.4(SMAD3):c.341A>G (p.Asn114Ser)	rs369221296	0.00001
NM_005902.4(SMAD3):c.1081G>A (p.Glu361Lys)	rs387906856
NM_005902.4(SMAD3):c.727C>G (p.Arg243Gly)	rs886039137

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