ClinVar Miner

List of variants in gene NIBAN1 reported as benign by Breakthrough Genomics, Breakthrough Genomics

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
NM_052966.4(NIBAN1):c.2488G>A (p.Gly830Ser)	rs35601690	0.02514
NM_052966.4(NIBAN1):c.558G>A (p.Arg186=)	rs116820598	0.01959

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