Variants in gene DOCK8 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 15

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HGVS	dbSNP	gnomAD frequency
NM_203447.4(DOCK8):c.4019A>G (p.Tyr1340Cys)	rs116920018	0.00276
NM_203447.4(DOCK8):c.380G>A (p.Arg127His)	rs150742426	0.00196
NM_203447.4(DOCK8):c.3460C>T (p.Arg1154Cys)	rs34390308	0.00170
NM_203447.4(DOCK8):c.452G>A (p.Arg151Gln)	rs149918318	0.00136
NM_203447.4(DOCK8):c.3988C>G (p.Leu1330Val)	rs148081681	0.00076
NM_203447.4(DOCK8):c.3263C>T (p.Thr1088Met)	rs149065013	0.00067
NM_203447.4(DOCK8):c.3023G>A (p.Arg1008Gln)	rs145844320	0.00064
NM_203447.4(DOCK8):c.494C>T (p.Ser165Leu)	rs146490788	0.00061
NM_203447.4(DOCK8):c.3312G>C (p.Glu1104Asp)	rs138810908	0.00054
NM_203447.4(DOCK8):c.3058A>G (p.Ile1020Val)	rs151094543	0.00046
NM_203447.4(DOCK8):c.2779A>G (p.Ile927Val)	rs759239515	0.00006
NM_203447.4(DOCK8):c.4346C>T (p.Ser1449Leu)	rs370123223	0.00006
NM_203447.4(DOCK8):c.1656A>G (p.Val552=)	rs150595667	0.00003
NM_203447.4(DOCK8):c.2017A>T (p.Ile673Phe)	rs372858877
NM_203447.4(DOCK8):c.2440+13_2440+22del	rs769837178

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