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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (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: 12

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HGVS	dbSNP	gnomAD frequency
NM_006516.4(SLC2A1):c.894C>T (p.Phe298=)	rs140825318	0.00073
NM_006516.4(SLC2A1):c.777C>T (p.Ile259=)	rs78388808	0.00068
NM_006516.4(SLC2A1):c.276-7T>C	rs369273744	0.00063
NM_006516.4(SLC2A1):c.498C>T (p.Val166=)	rs150971143	0.00036
NM_006516.4(SLC2A1):c.972+7del	rs531385270	0.00016
NM_006516.4(SLC2A1):c.987G>A (p.Glu329=)	rs201989024	0.00008
NM_006516.4(SLC2A1):c.258C>T (p.Phe86=)	rs147319894	0.00007
NM_006516.4(SLC2A1):c.1016T>C (p.Ile339Thr)	rs141619735	0.00006
NM_006516.4(SLC2A1):c.906G>T (p.Gly302=)	rs55693364	0.00004
NM_006516.4(SLC2A1):c.274C>A (p.Arg92=)	rs202060209
NM_006516.4(SLC2A1):c.679+4C>A	rs139492241
NM_006516.4(SLC2A1):c.679+4C>T	rs139492241

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