List of variants in gene SMAD3 reported as benign by Illumina Laboratory Services, Illumina

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_005902.4(SMAD3):c.309A>G (p.Leu103=)	rs1065080	0.87365
NM_005902.4(SMAD3):c.*2227G>A	rs11638476	0.31592
NM_005902.4(SMAD3):c.*2793C>T	rs3743342	0.19499
NM_005902.4(SMAD3):c.*2282C>T	rs12595334	0.19274
NM_005902.4(SMAD3):c.*1423C>T	rs2278670	0.19250
NM_005902.4(SMAD3):c.*1105G>A	rs8031440	0.19244
NM_005902.4(SMAD3):c.*1245G>A	rs8031627	0.19233
NM_005902.4(SMAD3):c.*402C>T	rs8025774	0.19194
NM_005902.4(SMAD3):c.508A>G (p.Ile170Val)	rs35874463	0.03414
NM_005902.4(SMAD3):c.*3512A>G	rs886051429
NM_005902.4(SMAD3):c.*3719C>T	rs886051431

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