ClinVar Miner

List of variants in gene combination CLASP1, RNU4ATAC reported as pathogenic by Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001395891.1(CLASP1):c.196-567G>A	rs559979281	0.00038
NR_023343.3(RNU4ATAC):n.51G>A	rs188343279	0.00038

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