ClinVar Miner

List of variants in gene combination COBLL1, SCN3A, SLC38A11 reported by Rare Disease Group, Clinical Genetics, Karolinska Institutet

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NC_000002.11:g.165492423_165973543dup

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