ClinVar Miner

List of variants in gene SLC9A1 reported as likely benign for Lichtenstein-Knorr syndrome

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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: 1

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HGVS	dbSNP	gnomAD frequency
NM_003047.5(SLC9A1):c.1821G>A (p.Gln607=)	rs139314838	0.00095

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