List of variants in gene SLC2A10 reported as likely pathogenic by CeGaT Center for Human Genetics 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_030777.4(SLC2A10):c.313C>T (p.Arg105Cys)	rs767864243	0.00005
NM_030777.4(SLC2A10):c.254T>C (p.Leu85Pro)	rs754120063
NM_030777.4(SLC2A10):c.395G>C (p.Arg132Pro)

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