List of variants in gene SBF2 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_030962.4(SBF2):c.93T>C (p.Phe31=)	rs200263159	0.00113
NM_030962.4(SBF2):c.1408C>A (p.Pro470Thr)	rs149967939	0.00052
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.1812C>T (p.Asp604=)	rs765658939	0.00015
NM_030962.4(SBF2):c.4095C>T (p.Ile1365=)	rs142904756	0.00011
NM_030962.4(SBF2):c.5469T>C (p.Arg1823=)	rs373457270	0.00002
NM_030962.4(SBF2):c.3618T>G (p.Val1206=)	rs1855446145
NM_030962.4(SBF2):c.3979-4G>A	rs375742620
NM_030962.4(SBF2):c.4444-9G>T	rs1185198722
NM_030962.4(SBF2):c.948A>G (p.Leu316=)	rs772340409
NM_030962.4(SBF2):c.960A>G (p.Gln320=)	rs2496157458

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