Variants in gene SBF1 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_002972.4(SBF1):c.4768A>G (p.Thr1590Ala)	rs200488568	0.00024
NM_002972.4(SBF1):c.1249A>G (p.Met417Val)	rs587776986	0.00001

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