List of variants in gene combination LOC113783876, VPS13B reported as uncertain significance 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_152564.5(VPS13B):c.-30T>A	rs886062533	0.00004
NM_152564.5(VPS13B):c.-30+5G>A
NM_152564.5(VPS13B):c.-30+6C>G	rs147672364

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