List of variants in gene SLC2A10 reported by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		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.1288+10G>A	rs76315093	0.00869
NM_030777.4(SLC2A10):c.674G>A (p.Arg225His)	rs34295241	0.00302
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.316G>T (p.Ala106Ser)	rs6094438
NM_030777.4(SLC2A10):c.510G>A (p.Trp170Ter)	rs80358229
NM_030777.4(SLC2A10):c.918C>T (p.Leu306=)	rs1979909437

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