List of variants in gene SBF2 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_030962.4(SBF2):c.*1364C>T	rs10118	0.63186
NM_030962.4(SBF2):c.*514C>T	rs3829252	0.33836
NM_030962.4(SBF2):c.*1515G>A	rs1045634	0.33744
NM_030962.4(SBF2):c.*40A>C	rs3751000	0.30738
NM_030962.4(SBF2):c.3646C>G (p.Gln1216Glu)	rs12574508	0.07978
NM_030962.4(SBF2):c.*1619A>C	rs360126	0.06256
NM_030962.4(SBF2):c.909C>T (p.Pro303=)	rs16907355	0.05858
NM_030962.4(SBF2):c.*1144A>G	rs3751001	0.04377
NM_030962.4(SBF2):c.*1399T>C	rs60154961	0.01504
NM_030962.4(SBF2):c.*1413A>G	rs59613534	0.01502
NM_030962.4(SBF2):c.*177A>C	rs192542785	0.00872
NM_030962.4(SBF2):c.*291C>T	rs114604750	0.00828
NM_030962.4(SBF2):c.*51T>C	rs41275194	0.00749
NM_030962.4(SBF2):c.1173A>G (p.Ala391=)	rs79470805	0.00687
NM_030962.4(SBF2):c.4096C>T (p.Pro1366Ser)	rs115927577	0.00548
NM_030962.4(SBF2):c.-118G>T	rs563422015	0.00491
NM_030962.4(SBF2):c.645T>C (p.Phe215=)	rs148187321	0.00491
NM_030962.4(SBF2):c.93T>C (p.Phe31=)	rs200263159	0.00003

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