List of variants in gene combination CHRNG, TIGD1 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_005199.5(CHRNG):c.1118G>A (p.Arg373Gln)	rs144755776	0.00019
NM_005199.5(CHRNG):c.1496G>A (p.Arg499Gln)	rs373096766	0.00003
NM_005199.5(CHRNG):c.1202A>G (p.Gln401Arg)	rs763132076	0.00001

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