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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (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: 5

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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.3460C>T (p.Arg1154Cys)	rs34390308	0.00170
NM_203447.4(DOCK8):c.3058A>G (p.Ile1020Val)	rs151094543	0.00046
NM_203447.4(DOCK8):c.828-7A>G	rs200243583	0.00030
NM_203447.4(DOCK8):c.3234+15dup	rs375864618

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