List of variants in gene SLC2A10 reported as likely benign by CeGaT Praxis fuer Humangenetik Tuebingen

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: 5

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HGVS	dbSNP
NM_030777.4(SLC2A10):c.1206T>A (p.Ala402=)
NM_030777.4(SLC2A10):c.1512G>A (p.Ser504=)	rs117587497
NM_030777.4(SLC2A10):c.1548G>T (p.Arg516=)	rs116344406
NM_030777.4(SLC2A10):c.237C>A (p.Leu79=)	rs201323237
NM_030777.4(SLC2A10):c.366C>T (p.Tyr122=)	rs34990188

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