List of variants in gene SBF2 reported as likely benign for not specified

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_030962.4(SBF2):c.4096C>T (p.Pro1366Ser)	rs115927577	0.00548
NM_030962.4(SBF2):c.777G>A (p.Pro259=)	rs142261202	0.00102
NM_030962.4(SBF2):c.4444-18T>G	rs143439179	0.00041
NM_030962.4(SBF2):c.1509A>G (p.Glu503=)	rs143773975	0.00030
NM_030962.4(SBF2):c.513+18A>T	rs201201683	0.00027
NM_030962.4(SBF2):c.4128G>A (p.Ala1376=)	rs191964053	0.00017
NM_030962.4(SBF2):c.4095C>T (p.Ile1365=)	rs142904756	0.00011
NM_030962.4(SBF2):c.403-15T>G	rs887143579	0.00003
NM_030962.4(SBF2):c.993G>A (p.Leu331=)	rs766193938	0.00003
NM_030962.4(SBF2):c.142-11A>G	rs539146891	0.00002
NM_030962.4(SBF2):c.402+15G>A	rs780717348	0.00002
NM_030962.4(SBF2):c.4068G>A (p.Leu1356=)	rs1429589073	0.00001
NM_030962.4(SBF2):c.4266C>T (p.Ser1422=)	rs763445946	0.00001
NM_030962.4(SBF2):c.4509C>T (p.His1503=)	rs138816399	0.00001
NM_030962.4(SBF2):c.620-9T>C	rs199676895	0.00001
NM_030962.4(SBF2):c.*20C>G	rs1057523279
NM_030962.4(SBF2):c.1054-11T>C	rs1554976748
NM_030962.4(SBF2):c.1110T>C (p.Tyr370=)	rs201361655
NM_030962.4(SBF2):c.1491T>C (p.Asn497=)	rs767806871
NM_030962.4(SBF2):c.1860+10A>G	rs778305149
NM_030962.4(SBF2):c.3652+6C>T	rs1057524041
NM_030962.4(SBF2):c.3979-4G>T	rs375742620
NM_030962.4(SBF2):c.492C>G (p.Val164=)	rs559769224
NM_030962.4(SBF2):c.753-16T>C	rs7128234
NM_030962.4(SBF2):c.807A>T (p.Pro269=)	rs1057521879
NM_030962.4(SBF2):c.862-9C>A	rs1554979581
NM_030962.4(SBF2):c.873C>T (p.Ile291=)	rs2134496815

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