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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC107303340, VHL
(L169P +1 more)
Single nucleotide variant
(missense variant +1 more)
Chuvash polycythemia
+2 more
GConflicting classifications of pathogenicity
LOC107303340, VHL
(I151T)
Single nucleotide variant
(missense variant +1 more)
Chuvash polycythemia
+3 more
GPathogenic