List of variants in gene SLC2A10 reported as uncertain significance by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_030777.4(SLC2A10):c.1370C>T (p.Ala457Val)	rs201393026	0.00015
NM_030777.4(SLC2A10):c.929C>T (p.Ser310Phe)	rs763521707	0.00003
NM_030777.4(SLC2A10):c.164T>C (p.Leu55Pro)	rs1555887820
NM_030777.4(SLC2A10):c.197G>A (p.Gly66Asp)	rs1555887829

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