ClinVar Miner

List of variants in gene combination INVS, LOC130002251 reported as benign by Genome Diagnostics Laboratory, The Hospital for Sick Children

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_014425.5(INVS):c.-110T>G	rs7024375	0.17693

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