List of variants in gene SLC2A10 reported as likely benign 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_030777.4(SLC2A10):c.674G>A (p.Arg225His)	rs34295241	0.00302
NM_030777.4(SLC2A10):c.816C>G (p.Ala272=)	rs148058006	0.00077
NM_030777.4(SLC2A10):c.765C>T (p.Ser255=)	rs142106322	0.00065
NM_030777.4(SLC2A10):c.1548-19C>T	rs144623242	0.00044
NM_030777.4(SLC2A10):c.1289-6C>T	rs199967429	0.00033
NM_030777.4(SLC2A10):c.180C>T (p.Leu60=)	rs371988251	0.00001

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