List of variants in gene DOCK2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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_004946.3(DOCK2):c.90G>C (p.Gln30His)	rs141894939	0.00226
NM_004946.3(DOCK2):c.279G>T (p.Thr93=)	rs144632263	0.00201
NM_004946.3(DOCK2):c.5446G>T (p.Ala1816Ser)	rs144315682	0.00151
NM_004946.3(DOCK2):c.5484G>A (p.Thr1828=)	rs140198889	0.00095
NM_004946.3(DOCK2):c.2638C>A (p.Leu880Met)	rs112062072	0.00060
NM_004946.3(DOCK2):c.1215C>T (p.Thr405=)	rs141406325	0.00032
NM_004946.3(DOCK2):c.3741C>T (p.His1247=)	rs144649763	0.00008
NM_004946.3(DOCK2):c.5130G>A (p.Ala1710=)	rs143741887	0.00006
NM_004946.3(DOCK2):c.5328G>A (p.Glu1776=)	rs958464049	0.00001
NM_004946.3(DOCK2):c.1843+8G>A	rs1581082214
NM_004946.3(DOCK2):c.3073-8A>G	rs113289730

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