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

rs387906503(-;T)

From SNPedia

deletion variant of uncertain significance
Is agenotype
ofrs387906503
GeneAGTR2
ChromosomeX
Position116,172,682
mentionedby
Magnitude1
Geno Mag Summary
(-;-) 1 deletion variant of uncertain significance
(-;T) 1 deletion variant of uncertain significance
(T;T) 0 common in clinvar

see rs387906503