List of variants in gene combination DOCK8, LOC130001437 reported as benign for hematologic disorder

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_203447.4(DOCK8):c.15G>A (p.Pro5=)	rs148276394	0.00188
NM_203447.4(DOCK8):c.8C>G (p.Thr3Ser)	rs199739266	0.00060

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