List of variants in gene SLC2A10 reported as benign for not specified

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_030777.4(SLC2A10):c.1547+18T>G	rs2425906	0.37194
NM_030777.4(SLC2A10):c.616G>A (p.Ala206Thr)	rs2235491	0.12316
NM_030777.4(SLC2A10):c.1541A>G (p.Lys514Arg)	rs41283344	0.06229
NM_030777.4(SLC2A10):c.1552A>G (p.Thr518Ala)	rs6018008	0.02748
NM_030777.4(SLC2A10):c.1609A>G (p.Ile537Val)	rs7348121	0.02113
NM_030777.4(SLC2A10):c.1154C>G (p.Ala385Gly)	rs79849424	0.01835
NM_030777.4(SLC2A10):c.-27C>T	rs149481442	0.01295
NM_030777.4(SLC2A10):c.1288+10G>A	rs76315093	0.00869
NM_030777.4(SLC2A10):c.1548-18G>A	rs113496485	0.00749
NM_030777.4(SLC2A10):c.1617G>A (p.Ala539=)	rs114974138	0.00514
NM_030777.4(SLC2A10):c.366C>T (p.Tyr122=)	rs34990188	0.00411
NM_030777.4(SLC2A10):c.1212G>T (p.Gly404=)	rs139155480	0.00363
NM_030777.4(SLC2A10):c.674G>A (p.Arg225His)	rs34295241	0.00302
NM_030777.4(SLC2A10):c.1548G>T (p.Arg516=)	rs116344406	0.00241
NM_030777.4(SLC2A10):c.-15C>T	rs377142129	0.00166
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.1548-19C>T	rs144623242	0.00044
NM_030777.4(SLC2A10):c.1289-6C>T	rs199967429	0.00033
NM_030777.4(SLC2A10):c.1008C>T (p.Thr336=)	rs370173604	0.00019
NM_030777.4(SLC2A10):c.1593G>A (p.Pro531=)	rs148424607	0.00019
NM_030777.4(SLC2A10):c.780C>T (p.Ser260=)	rs181500247	0.00016
NM_030777.4(SLC2A10):c.237C>T (p.Leu79=)	rs201323237
NM_030777.4(SLC2A10):c.316G>T (p.Ala106Ser)	rs6094438

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