Variants in gene SLC2A10 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_030777.4(SLC2A10):c.394C>T (p.Arg132Trp)	rs121908173	0.00010
NM_030777.4(SLC2A10):c.691C>T (p.Arg231Trp)	rs146579504	0.00010
NM_030777.4(SLC2A10):c.313C>T (p.Arg105Cys)	rs767864243	0.00005
NM_030777.4(SLC2A10):c.1276G>T (p.Gly426Trp)	rs121908172	0.00004
NM_030777.4(SLC2A10):c.1330C>T (p.Arg444Ter)	rs370547023	0.00002
NM_030777.4(SLC2A10):c.692G>A (p.Arg231Gln)	rs771028960	0.00002
NM_030777.4(SLC2A10):c.648C>G (p.Tyr216Ter)	rs1015798796	0.00001
NM_030777.4(SLC2A10):c.243C>G (p.Ser81Arg)	rs80358230

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