List of variants in gene SLC2A1 reported as benign by Eurofins NTD LLC (GA)

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_006516.4(SLC2A1):c.45C>T (p.Ala15=)	rs1385129	0.21537
NM_006516.4(SLC2A1):c.399C>T (p.Cys133=)	rs11537641	0.16943
NM_006516.4(SLC2A1):c.966C>T (p.Val322=)	rs2229680	0.06553
NM_006516.4(SLC2A1):c.1065A>G (p.Leu355=)	rs2228490	0.04552
NM_006516.4(SLC2A1):c.19-207T>C	rs41310434	0.01173
NM_006516.4(SLC2A1):c.973-17A>G	rs111596088	0.01025
NM_006516.4(SLC2A1):c.417C>T (p.Phe139=)	rs144538918	0.00517
NM_006516.4(SLC2A1):c.1296C>T (p.Tyr432=)	rs75485205	0.00267
NM_006516.4(SLC2A1):c.27G>A (p.Thr9=)	rs34025424	0.00176
NM_006516.4(SLC2A1):c.1170C>T (p.Ile390=)	rs2236574	0.00081
NM_006516.4(SLC2A1):c.1372C>A (p.Arg458=)	rs13306758	0.00070
NM_006516.4(SLC2A1):c.1011C>T (p.His337=)	rs2229681
NM_006516.4(SLC2A1):c.588G>A (p.Pro196=)	rs2229682
NM_006516.4(SLC2A1):c.679+7G>C	rs13306757
NM_006516.4(SLC2A1):c.679+7G>T	rs13306757

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