Variants in gene SLC2A1 with conflicting interpretations "uncertain significance" and "pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_006516.4(SLC2A1):c.278G>A (p.Arg93Gln)	rs80359815	0.00001
NM_006516.4(SLC2A1):c.1131CTT[1] (p.Phe379del)
NM_006516.4(SLC2A1):c.1232A>G (p.Asn411Ser)	rs398123069
NM_006516.4(SLC2A1):c.1402C>T (p.Arg468Trp)	rs267607059
NM_006516.4(SLC2A1):c.203C>T (p.Ser68Leu)	rs1570593865
NM_006516.4(SLC2A1):c.458G>A (p.Arg153His)	rs794727642
NM_006516.4(SLC2A1):c.766_767delinsGT (p.Lys256Val)	rs80359822
NM_006516.4(SLC2A1):c.877T>C (p.Tyr293His)	rs2124448410

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