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rs104893831(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs104893831
GeneVHL
Chromosome3
Position10,146,549
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 7 Von Hippel-Lindau syndrome mutation