List of variants in gene SMAD3 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_005902.4(SMAD3):c.-265T>G	rs886051373	0.00017
NM_005902.4(SMAD3):c.1070A>G (p.Asn357Ser)	rs140880290	0.00003
NM_005902.4(SMAD3):c.1258C>T (p.Arg420Cys)	rs1206533102	0.00003
NM_005902.4(SMAD3):c.394A>G (p.Thr132Ala)	rs371876622	0.00003
NM_005902.4(SMAD3):c.334G>A (p.Ala112Thr)	rs770798158	0.00002
NM_005902.4(SMAD3):c.643G>A (p.Ala215Thr)	rs1962721856	0.00001
NM_005902.4(SMAD3):c.-164A>C	rs886051378
NM_005902.4(SMAD3):c.238C>T (p.Arg80Trp)	rs750707381
NM_005902.4(SMAD3):c.317T>C (p.Met106Thr)	rs1301737199
NM_005902.4(SMAD3):c.401-6G>A	rs745672741
NM_005902.4(SMAD3):c.448T>C (p.Phe150Leu)	rs751860407
NM_005902.4(SMAD3):c.908T>A (p.Val303Asp)	rs1555414011
NM_005902.4(SMAD3):c.934G>A (p.Ala312Thr)	rs750756638
NM_005902.4(SMAD3):c.967C>T (p.Arg323Cys)	rs967072552

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