List of variants in gene SLC2A10 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_030777.4(SLC2A10):c.1547+18T>G	rs2425906	0.37194
NM_030777.4(SLC2A10):c.616G>A (p.Ala206Thr)	rs2235491	0.12316
NM_030777.4(SLC2A10):c.1541A>G (p.Lys514Arg)	rs41283344	0.06229
NM_030777.4(SLC2A10):c.1552A>G (p.Thr518Ala)	rs6018008	0.02748
NM_030777.4(SLC2A10):c.1609A>G (p.Ile537Val)	rs7348121	0.02113
NM_030777.4(SLC2A10):c.1154C>G (p.Ala385Gly)	rs79849424	0.01835
NM_030777.4(SLC2A10):c.1288+10G>A	rs76315093	0.00869
NM_030777.4(SLC2A10):c.1548-18G>A	rs113496485	0.00749
NM_030777.4(SLC2A10):c.1617G>A (p.Ala539=)	rs114974138	0.00514
NM_030777.4(SLC2A10):c.366C>T (p.Tyr122=)	rs34990188	0.00411

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