ClinVar Miner

List of variants in gene combination ANK1, LOC124153154 reported as uncertain significance by Revvity Omics, Revvity

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_000037.4(ANK1):c.499G>C (p.Gly167Arg)	rs201024919	0.00021
NM_000037.4(ANK1):c.563C>T (p.Thr188Met)	rs146346710	0.00004

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