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rs121908829(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs121908829
GeneTMEM127
Chromosome2
Position96,254,078
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 6.2 Hereditary PGL/PCC Syndrome
(G;G) 0 common in clinvar