List of variants in gene SLC2A2 reported as benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000340.2(SLC2A2):c.1437C>T (p.Phe479=)	rs5398	0.38373
NM_000340.2(SLC2A2):c.329C>T (p.Thr110Ile)	rs5400	0.23124
NM_000340.2(SLC2A2):c.496+8A>T	rs5402	0.22868
NM_000340.2(SLC2A2):c.776-15C>T	rs5406	0.21500
NM_000340.2(SLC2A2):c.594G>A (p.Thr198=)	rs5404	0.15665
NM_000340.2(SLC2A2):c.1069-9T>C	rs5407	0.01360
NM_000340.2(SLC2A2):c.661C>T (p.Leu221=)	rs5405	0.00373
NM_000340.2(SLC2A2):c.301G>A (p.Val101Ile)	rs1800572	0.00061
NM_000340.2(SLC2A2):c.*8del (p.Ter525=)	rs573575421
NM_000340.2(SLC2A2):c.496+7_496+8insCTCA	rs746295534

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