List of variants in gene DOK7 reported as benign by Eurofins NTD LLC (GA)

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_173660.5(DOK7):c.1382G>A (p.Gly461Asp)	rs9684786	0.20663
NM_173660.5(DOK7):c.1185C>T (p.Tyr395=)	rs6850908	0.18472
NM_173660.5(DOK7):c.887A>G (p.Gln296Arg)	rs6811423	0.18249
NM_173660.5(DOK7):c.1113A>C (p.Ser371=)	rs6811856	0.18181
NM_173660.5(DOK7):c.1134G>A (p.Ala378=)	rs6831659	0.17563
NM_173660.5(DOK7):c.1243C>T (p.Pro415Ser)	rs16844464	0.06297
NM_173660.5(DOK7):c.-6C>G	rs191800156	0.01785
NM_173660.5(DOK7):c.1351C>T (p.Arg451Trp)	rs16844470	0.01433
NM_173660.5(DOK7):c.1143C>T (p.Pro381=)	rs56769879	0.01415
NM_173660.5(DOK7):c.1295G>A (p.Arg432Lys)	rs145419117	0.00243
NM_173660.5(DOK7):c.220= (p.Leu74=)	rs4325970

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