List of variants in gene combination LOC107303340, VHL reported as likely pathogenic for bone disorder

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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_000551.4(VHL):c.562C>G (p.Leu188Val)	rs5030824	0.00004
NM_000551.4(VHL):c.628C>T (p.Arg210Trp)	rs774380450	0.00002
NM_000551.4(VHL):c.538A>G (p.Ile180Val)	rs377715747	0.00001

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