List of variants in gene SLC2A10 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_030777.4(SLC2A10):c.515C>T (p.Thr172Ile)	rs143301610	0.00100
NM_030777.4(SLC2A10):c.931G>A (p.Val311Ile)	rs139932041	0.00026
NM_030777.4(SLC2A10):c.317C>G (p.Ala106Gly)	rs144095826	0.00023
NM_030777.4(SLC2A10):c.1370C>T (p.Ala457Val)	rs201393026	0.00015
NM_030777.4(SLC2A10):c.115G>A (p.Asp39Asn)	rs367623970	0.00004
NM_030777.4(SLC2A10):c.1351T>G (p.Cys451Gly)	rs199599532	0.00003
NM_030777.4(SLC2A10):c.316G>A (p.Ala106Thr)	rs6094438
NM_030777.4(SLC2A10):c.356G>A (p.Cys119Tyr)
NM_030777.4(SLC2A10):c.632C>T (p.Pro211Leu)	rs151324893

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