List of variants in gene SMAD3 reported as likely benign for not specified

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_005902.4(SMAD3):c.316A>G (p.Met106Val)	rs138550573	0.00099
NM_005902.4(SMAD3):c.607+7C>T	rs200998367	0.00036
NM_005902.4(SMAD3):c.636G>A (p.Met212Ile)	rs202094530	0.00016
NM_005902.4(SMAD3):c.984G>A (p.Pro328=)	rs150994304	0.00016
NM_005902.4(SMAD3):c.885G>A (p.Arg295=)	rs139616052	0.00009
NM_005902.4(SMAD3):c.933C>T (p.Ser311=)	rs771384141	0.00008
NM_005902.4(SMAD3):c.207-26869C>A	rs958007552	0.00006
NM_005902.4(SMAD3):c.990C>T (p.Thr330=)	rs774470515	0.00006
NM_005902.4(SMAD3):c.1125C>T (p.Ser375=)	rs144245324	0.00004
NM_005902.4(SMAD3):c.608-15T>C	rs371614939	0.00004
NM_005902.4(SMAD3):c.1102C>A (p.Arg368=)	rs757106110	0.00003
NM_005902.4(SMAD3):c.207-4G>A	rs1319147414	0.00003
NM_005902.4(SMAD3):c.608-4G>A	rs372064378	0.00002
NM_005902.4(SMAD3):c.1009+11C>T	rs774180178	0.00001
NM_005902.4(SMAD3):c.381C>T (p.Tyr127=)	rs886038971	0.00001
NM_005902.4(SMAD3):c.462C>T (p.Asp154=)	rs756124653	0.00001
NM_005902.4(SMAD3):c.501C>T (p.Pro167=)	rs138395233	0.00001
NM_005902.4(SMAD3):c.603C>T (p.Asp201=)	rs774814963	0.00001
NM_005902.4(SMAD3):c.657G>C (p.Leu219Phe)	rs886038567	0.00001
NM_005902.4(SMAD3):c.400+14C>T	rs1555412095
NM_005902.4(SMAD3):c.441G>A (p.Pro147=)	rs140275295
NM_005902.4(SMAD3):c.45G>C (p.Leu15=)
NM_005902.4(SMAD3):c.543C>T (p.Pro181=)	rs1026881356
NM_005902.4(SMAD3):c.658+18C>A	rs1057521458
NM_005902.4(SMAD3):c.872-15C>T	rs747102986

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