List of variants in gene ATRNL1 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
GRCh37/hg19 10q25.3(chr10:117203412-117239047)x1
GRCh38/hg38 10q25.3(chr10:115124875-115304059)x1
GRCh38/hg38 10q25.3(chr10:115174050-115304059)x1

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