Variants in gene SPRED1 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 12

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HGVS	dbSNP	gnomAD frequency
NM_152594.3(SPRED1):c.926T>C (p.Val309Ala)	rs114636635	0.00204
NM_152594.3(SPRED1):c.675C>T (p.Ser225=)	rs144764225	0.00092
NM_152594.3(SPRED1):c.207+15A>G	rs377288061	0.00073
NM_152594.3(SPRED1):c.939G>A (p.Thr313=)	rs140644874	0.00070
NM_152594.3(SPRED1):c.30C>A (p.Asn10Lys)	rs201692618	0.00042
NM_152594.3(SPRED1):c.377-10A>G	rs376134678	0.00026
NM_152594.3(SPRED1):c.124G>A (p.Val42Ile)	rs147204964	0.00017
NM_152594.3(SPRED1):c.963G>A (p.Lys321=)	rs369711772	0.00011
NM_152594.3(SPRED1):c.26A>T (p.Asp9Val)	rs200157475	0.00010
NM_152594.3(SPRED1):c.685-8T>C	rs760690837	0.00005
NM_152594.3(SPRED1):c.879G>A (p.Leu293=)	rs535687467	0.00002
NM_152594.3(SPRED1):c.207+37A>G	rs2272105

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