ClinVar Miner

List of variants in gene combination AKAP17A, ASMT, ASMTL, CRLF2, CSF2RA, IL3RA, LINC00106, MIR3690, P2RY8, SLC25A6 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 Xp22.33(chrX:1000807-1702424)x3
GRCh38/hg38 Xp22.33(chrX:1063677-1838017)x3
GRCh38/hg38 Yp11.2(chrY:1112351-1702424)x3

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