List of variants in gene combination LOC107303340, VHL reported as not provided 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_000551.4(VHL):c.340+578C>T	rs139622356	0.00064
NM_000551.4(VHL):c.439A>G (p.Ile147Val)	rs1057517560	0.00002

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