Variants in gene SLC25A15 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_014252.4(SLC25A15):c.182G>A (p.Arg61His)	rs34615430	0.00292
NM_014252.4(SLC25A15):c.564C>T (p.Phe188=)	rs141028076	0.00077
NM_014252.4(SLC25A15):c.345C>T (p.Phe115=)	rs35434090	0.00029
NM_014252.4(SLC25A15):c.706A>G (p.Arg236Gly)	rs142236568	0.00012
NM_014252.4(SLC25A15):c.216C>T (p.Ile72=)	rs572717478	0.00011
NM_014252.4(SLC25A15):c.278G>A (p.Arg93Gln)	rs369201060	0.00010
NM_014252.4(SLC25A15):c.861C>T (p.Tyr287=)	rs148422923	0.00010
NM_014252.4(SLC25A15):c.147C>G (p.Asp49Glu)	rs187685447	0.00009
NM_014252.4(SLC25A15):c.381G>A (p.Thr127=)	rs543205273	0.00005
NM_014252.4(SLC25A15):c.388G>A (p.Val130Met)	rs553432772	0.00005
NM_014252.4(SLC25A15):c.417G>A (p.Glu139=)	rs752316567	0.00005
NM_014252.4(SLC25A15):c.255C>T (p.Tyr85=)	rs536354947	0.00004
NM_014252.4(SLC25A15):c.225C>T (p.Ile75=)	rs765380976	0.00001
NM_014252.4(SLC25A15):c.45G>A (p.Ala15=)	rs200958757

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