ClinVar Miner

List of variants in gene combination PSMC2, SLC26A5 reported as benign

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NC_000007.14:g.103352579A>G	rs11978339	0.21690
NC_000007.14:g.103352638C>T	rs35850434	0.16295

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