List of variants reported as likely benign for Chuvash polycythemia; Pheochromocytoma; Von Hippel-Lindau syndrome; Nonpapillary renal cell carcinoma

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
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.340+578C>T	rs139622356	0.00064
NM_000551.4(VHL):c.5C>T (p.Pro2Leu)	rs111246617	0.00008
NM_000551.4(VHL):c.420C>A (p.Leu140=)	rs369465430	0.00004
NM_000551.4(VHL):c.267C>A (p.Leu89=)	rs755794553	0.00002
NM_000551.4(VHL):c.426T>C (p.Val142=)	rs143594610	0.00001
NM_000551.4(VHL):c.-10C>T	rs1192379474
NM_000551.4(VHL):c.463+9G>A	rs1057522720

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