Variants in gene ROGDI 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_024589.3(ROGDI):c.414G>A (p.Thr138=)	rs11553876	0.10521
NM_024589.3(ROGDI):c.433-15C>T	rs114103417	0.00806
NM_024589.3(ROGDI):c.713G>A (p.Arg238His)	rs138409264	0.00548
NM_024589.3(ROGDI):c.522C>T (p.Ser174=)	rs150687774	0.00190
NM_024589.3(ROGDI):c.118-13C>G	rs201794245	0.00137
NM_024589.3(ROGDI):c.532-4G>A	rs3747610	0.00017
NM_024589.3(ROGDI):c.696-8G>T	rs3747609	0.00008
NM_024589.3(ROGDI):c.823-10C>T	rs199642172	0.00007
NM_024589.3(ROGDI):c.117+10C>G	rs113858060

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