List of variants in gene SMC1A 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: 18

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HGVS	dbSNP	gnomAD frequency
NM_006306.4(SMC1A):c.-19C>T	rs1264011	0.42752
NM_006306.4(SMC1A):c.*5481G>A	rs147896900	0.01746
NM_006306.4(SMC1A):c.412-10C>T	rs149219651	0.01511
NM_006306.4(SMC1A):c.*2423G>A	rs147324052	0.00991
NM_006306.4(SMC1A):c.*5016T>C	rs17002602	0.00919
NM_006306.4(SMC1A):c.*2389G>T	rs114329529	0.00775
NM_006306.4(SMC1A):c.1698G>A (p.Glu566=)	rs7052858	0.00452
NM_006306.4(SMC1A):c.*4887T>C	rs142173620	0.00318
NM_006306.4(SMC1A):c.*3421G>T	rs41304780	0.00288
NM_006306.4(SMC1A):c.*1542T>C	rs781783328	0.00263
NM_006306.4(SMC1A):c.1254+11G>C	rs144354524	0.00258
NM_006306.4(SMC1A):c.3450C>T (p.Ala1150=)	rs142611198	0.00183
NM_006306.4(SMC1A):c.*5444G>A	rs181871602	0.00055
NM_006306.4(SMC1A):c.*1239T>C	rs782502306	0.00023
NM_006306.4(SMC1A):c.*3851A>T	rs782817464	0.00023
NM_006306.4(SMC1A):c.1173G>A (p.Gln391=)	rs147952638	0.00019
NM_006306.4(SMC1A):c.*2856A>T	rs148128199	0.00018
NM_006306.4(SMC1A):c.*931A>G	rs782237045	0.00001

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