List of variants in gene combination DOK7, LOC129992118 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_173660.5(DOK7):c.752C>T (p.Ala251Val)	rs376251309	0.00013
NM_173660.5(DOK7):c.731G>A (p.Arg244Gln)	rs755873468	0.00009
NM_173660.5(DOK7):c.689G>A (p.Arg230His)	rs760941977	0.00002
NM_173660.5(DOK7):c.766A>G (p.Ser256Gly)	rs750004938	0.00001
NM_173660.5(DOK7):c.761C>G (p.Pro254Arg)	rs200407250
NM_173660.5(DOK7):c.761C>T (p.Pro254Leu)	rs200407250

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