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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_152594.3(SPRED1):c.944C>T (p.Pro315Leu)	rs115440602	0.00029
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.587C>T (p.Thr196Ile)	rs147474792	0.00008
NM_152594.3(SPRED1):c.634G>A (p.Val212Ile)	rs769630742	0.00004
NM_152594.3(SPRED1):c.684+50A>T	rs200338097	0.00003
NM_152594.3(SPRED1):c.196A>C (p.Arg66=)	rs751923342	0.00001
NM_152594.3(SPRED1):c.211G>A (p.Val71Ile)	rs369150309	0.00001

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