ClinVar Miner

List of variants in gene combination TM4SF19, TM4SF19-DYNLT2B reported as likely benign for not provided

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
NC_000003.12:g.196320042A>C	rs1024531445	0.00001
NC_000003.12:g.196320048T>G	rs1187330028	0.00001

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