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rs5030819(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs5030819
GeneVHL
Chromosome3
Position10,149,813
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 7 Von Hippel-Lindau syndrome mutation