List of variants in gene VHL reported as benign for immune system 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: 9

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HGVS	dbSNP	gnomAD frequency
NC_000003.12:g.10141653G>A	rs779805	0.56161
NM_000551.4(VHL):c.74C>T (p.Pro25Leu)	rs35460768	0.00261
NM_000551.4(VHL):c.340+5G>C	rs61758376	0.00190
NC_000003.12:g.10141751T>G	rs34271731	0.00106
NM_000551.4(VHL):c.-5A>C	rs35793832	0.00106
NM_000551.4(VHL):c.150C>G (p.Ala50=)	rs61751580	0.00070
NM_000551.4(VHL):c.183C>G (p.Pro61=)	rs63650860	0.00067
NM_000551.4(VHL):c.241C>T (p.Pro81Ser)	rs104893829	0.00039
NM_000551.4(VHL):c.183C>T (p.Pro61=)	rs63650860

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