List of variants in gene combination LOC116268437, SYT10 reported as uncertain significance by ISCA site 1

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: 3

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HGVS	dbSNP	gnomAD frequency
GRCh38/hg38 12p11.1(chr12:33276356-33734564)x1
GRCh38/hg38 12p11.1(chr12:33387634-33973022)x1
GRCh38/hg38 12p11.1(chr12:33392214-33943704)x1

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