Have questions? Visit https://www.reddit.com/r/SNPedia

rs121908826(A;A)

From SNPedia
common in complete genomics
Is agenotype
ofrs121908826
GeneTMEM127
Chromosome2
Position96,254,117
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 0 common in complete genomics
(A;C) 6.2 Hereditary PGL/PCC Syndrome

Retrieved from "https://www.SNPedia.com/index.php?title=Rs121908826(A;A)&oldid=544543"
Powered by MediaWiki
Powered by Semantic MediaWiki
Powered by the NCBI