List of variants in gene DOCK2 reported as likely pathogenic by Invitae

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_004946.3(DOCK2):c.3310C>T (p.Arg1104Trp)	rs780318765	0.00001
NM_004946.3(DOCK2):c.1055+1G>A
NM_004946.3(DOCK2):c.1843+1G>T	rs1761749097
NM_004946.3(DOCK2):c.321+1G>A	rs1561585424
NM_004946.3(DOCK2):c.3381+2T>C	rs1581531492
NM_004946.3(DOCK2):c.3756+2T>C	rs1035797449
NM_004946.3(DOCK2):c.4072-1G>C
NM_004946.3(DOCK2):c.4213+1G>A	rs1561898523
NM_004946.3(DOCK2):c.5288-1G>T
NM_004946.3(DOCK2):c.606+2T>G

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