List of variants in gene DOCK6 reported as likely pathogenic for not provided

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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: 27

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HGVS	dbSNP	gnomAD frequency
NM_020812.4(DOCK6):c.5939+2T>C	rs201387914	0.00019
NM_020812.4(DOCK6):c.3562C>T (p.Gln1188Ter)	rs372751467	0.00001
NM_020812.4(DOCK6):c.1024-2A>T	rs1170041461
NM_020812.4(DOCK6):c.1104+2T>C	rs754888606
NM_020812.4(DOCK6):c.1105-1G>T
NM_020812.4(DOCK6):c.1832+1G>A
NM_020812.4(DOCK6):c.1971+1G>T
NM_020812.4(DOCK6):c.1972-2A>G	rs2147832572
NM_020812.4(DOCK6):c.2160+1G>A
NM_020812.4(DOCK6):c.2393-2A>C
NM_020812.4(DOCK6):c.2719-1G>C	rs2147805055
NM_020812.4(DOCK6):c.3241-1G>C
NM_020812.4(DOCK6):c.3241-2A>T
NM_020812.4(DOCK6):c.3380+2T>G
NM_020812.4(DOCK6):c.44+1G>T
NM_020812.4(DOCK6):c.44+2T>C
NM_020812.4(DOCK6):c.4650+1_4650+3del	rs1280482569
NM_020812.4(DOCK6):c.5235+1_5235+7del
NM_020812.4(DOCK6):c.5414_5415del (p.Asp1804_Ser1805insTer)
NM_020812.4(DOCK6):c.5451+1G>A
NM_020812.4(DOCK6):c.5452-2A>G
NM_020812.4(DOCK6):c.5689-2_5699del
NM_020812.4(DOCK6):c.5764C>T (p.Gln1922Ter)	rs2147691056
NM_020812.4(DOCK6):c.631del (p.Ala211fs)	rs761856660
NM_020812.4(DOCK6):c.705C>G (p.Tyr235Ter)	rs1555697020
NM_020812.4(DOCK6):c.806+1G>C
NM_020812.4(DOCK6):c.807-1G>A

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