List of variants in gene SLC2A10 reported as likely benign by Genome Diagnostics Laboratory, Amsterdam University Medical Center

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	gnomAD frequency
NM_030777.4(SLC2A10):c.1512G>A (p.Ser504=)	rs117587497	0.00128
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.330C>T (p.Phe110=)	rs199848479	0.00010
NM_030777.4(SLC2A10):c.306C>T (p.Val102=)	rs530216827	0.00003

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