List of variants in gene SMAD3 reported as benign for not provided

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: 32

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HGVS	dbSNP	gnomAD frequency
NM_005902.4(SMAD3):c.207-26500T>C	rs959504	0.96997
NM_005902.4(SMAD3):c.207-27010T>C	rs1866318	0.96991
NM_005902.4(SMAD3):c.533-187C>T	rs7179840	0.67237
NM_005902.4(SMAD3):c.400+59G>C	rs2289261	0.61732
NM_005902.4(SMAD3):c.1009+248C>T	rs55894213	0.46065
NM_005902.4(SMAD3):c.*2227G>A	rs11638476	0.31592
NM_005902.4(SMAD3):c.207-38842A>G	rs4776342	0.29814
NM_005902.4(SMAD3):c.207-39000G>A	rs8028147	0.29657
NM_005902.4(SMAD3):c.207-39129G>A	rs11636161	0.25577
NM_005902.4(SMAD3):c.872-113G>T	rs2289791	0.22527
NM_005902.4(SMAD3):c.872-95T>C	rs2289790	0.22233
NM_005902.4(SMAD3):c.872-330G>A	rs7181877	0.21605
NM_005902.4(SMAD3):c.872-297C>T	rs7181556	0.21538
NM_005902.4(SMAD3):c.872-309C>T	rs7181543	0.21340
NM_005902.4(SMAD3):c.533-478T>C	rs17228212	0.20997
NM_005902.4(SMAD3):c.*2282C>T	rs12595334	0.19274
NM_005902.4(SMAD3):c.532+128G>A	rs2289259	0.16225
NM_005902.4(SMAD3):c.533-104C>T	rs7179893	0.15834
NM_005902.4(SMAD3):c.207-39028G>A	rs16950635	0.07150
NM_005902.4(SMAD3):c.207-26681T>C	rs12914140	0.06825
NM_005902.4(SMAD3):c.1155-55A>G	rs28410524	0.01927
NM_005902.4(SMAD3):c.1009+69G>C	rs58056680	0.01875
NM_005902.4(SMAD3):c.1155-54C>T	rs28774694	0.01542
NM_005902.4(SMAD3):c.207-26896G>A	rs146714608	0.01070
NM_005902.4(SMAD3):c.636G>A (p.Met212Ile)	rs202094530	0.00016
NM_005902.4(SMAD3):c.607+9T>A	rs886051380	0.00005
NM_005902.4(SMAD3):c.400+58dup	rs72661155
NM_005902.4(SMAD3):c.533-589G>A	rs112991343
NM_005902.4(SMAD3):c.659-268TAAA[10]	rs60300820
NM_005902.4(SMAD3):c.659-268TAAA[11]	rs60300820
NM_005902.4(SMAD3):c.659-268TAAA[7]	rs60300820
NM_005902.4(SMAD3):c.659-268TAAA[8]	rs60300820

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