List of variants in gene SLC2A10 reported as benign by Illumina Laboratory Services, Illumina

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_030777.4(SLC2A10):c.*2176T>C	rs1059217	0.40292
NM_030777.4(SLC2A10):c.*2285T>G	rs1136540	0.40283
NM_030777.4(SLC2A10):c.*2365T>A	rs1136544	0.38922
NM_030777.4(SLC2A10):c.*1293T>C	rs707507	0.38336
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.*56A>G	rs112821000	0.02108
NM_030777.4(SLC2A10):c.1154C>G (p.Ala385Gly)	rs79849424	0.01835
NM_030777.4(SLC2A10):c.*143G>A	rs35691491	0.01384
NM_030777.4(SLC2A10):c.*280C>T	rs6018009	0.01365
NM_030777.4(SLC2A10):c.*334A>G	rs6018010	0.01363
NM_030777.4(SLC2A10):c.-27C>T	rs149481442	0.01295
NM_030777.4(SLC2A10):c.*1100T>G	rs6094450	0.00880
NM_030777.4(SLC2A10):c.1288+10G>A	rs76315093	0.00869
NM_030777.4(SLC2A10):c.*50T>C	rs36103903	0.00858
NM_030777.4(SLC2A10):c.*478G>A	rs113058599	0.00747
NM_030777.4(SLC2A10):c.*32T>C	rs78864327	0.00746
NM_030777.4(SLC2A10):c.*513T>C	rs111352987	0.00743
NM_030777.4(SLC2A10):c.*641G>A	rs113629687	0.00741
NM_030777.4(SLC2A10):c.*809C>T	rs114681513	0.00646
NM_030777.4(SLC2A10):c.*958C>T	rs189464814	0.00562
NM_030777.4(SLC2A10):c.1617G>A (p.Ala539=)	rs114974138	0.00514
NM_030777.4(SLC2A10):c.1212G>T (p.Gly404=)	rs139155480	0.00363
NM_030777.4(SLC2A10):c.316G>T (p.Ala106Ser)	rs6094438

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