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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_030777.4(SLC2A10):c.1547+223G>T	rs3091961	0.38349
NM_030777.4(SLC2A10):c.1547+96C>T	rs2425907	0.37632
NM_030777.4(SLC2A10):c.1412-114A>G	rs1122067	0.37139
NM_030777.4(SLC2A10):c.1411+175_1411+176insTTTTACATCA	rs199896452	0.04770
NM_030777.4(SLC2A10):c.1411+176G>C	rs775643873	0.04768
NM_030777.4(SLC2A10):c.1411+181del	rs201022621	0.04767
NM_030777.4(SLC2A10):c.1547+155T>G	rs1031479402	0.03288
NM_030777.4(SLC2A10):c.*56A>G	rs112821000	0.02108
NM_030777.4(SLC2A10):c.1212G>T (p.Gly404=)	rs139155480	0.00363
NM_030777.4(SLC2A10):c.-22A>G	rs886056723	0.00001
NM_030777.4(SLC2A10):c.5-165GGAT[10]	rs3092014
NM_030777.4(SLC2A10):c.5-165GGAT[11]	rs3092014
NM_030777.4(SLC2A10):c.5-165GGAT[9]	rs3092014
NM_030777.4(SLC2A10):c.5-234GGAT[11]	rs111504264
NM_030777.4(SLC2A10):c.5-234GGAT[9]	rs111504264

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