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rs753021890

From SNPedia

ClinVar
Risk rs753021890(A;A) rs753021890(T;T)
Alt rs753021890(A;A) rs753021890(T;T)
Reference rs753021890(G;G)
Significance Pathogenic
Disease Glaucoma 3
Variation info
Gene TEK
CLNDBN Glaucoma 3, primary congenital, E
Reversed 0
HGVS NC_000009.11:g.27168576G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000415600.1,