List of variants in gene DOCK2 reported as likely benign for DOCK2-related condition

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_004946.3(DOCK2):c.631A>G (p.Met211Val)	rs151191554	0.00305
NM_004946.3(DOCK2):c.90G>C (p.Gln30His)	rs141894939	0.00226
NM_004946.3(DOCK2):c.1360G>A (p.Ala454Thr)	rs114888195	0.00210
NM_004946.3(DOCK2):c.753G>A (p.Thr251=)	rs146746458	0.00113
NM_004946.3(DOCK2):c.2587A>G (p.Lys863Glu)	rs141501849	0.00100
NM_004946.3(DOCK2):c.5484G>A (p.Thr1828=)	rs140198889	0.00095
NM_004946.3(DOCK2):c.3836C>T (p.Thr1279Met)	rs145873210	0.00066
NM_004946.3(DOCK2):c.3756+9A>T	rs570358398	0.00021
NM_004946.3(DOCK2):c.2704-3C>T	rs144101028	0.00006
NM_004946.3(DOCK2):c.1437T>C (p.Val479=)	rs147336443	0.00001
NM_004946.3(DOCK2):c.1716A>T (p.Arg572=)
NM_004946.3(DOCK2):c.4449G>A (p.Glu1483=)
NM_004946.3(DOCK2):c.660C>A (p.Thr220=)

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