rs169311, None

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Alopecia, Male Pattern
CUI: C4083212
Disease: Alopecia, Male Pattern
0.700 GeneticVariation GWASDB Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases. 22693459 2012
Androgen-Insensitivity Syndrome
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
0.010 GeneticVariation BEFREE Moreover, rs169311 could be a functional variant regulating the expression of PAX1 in the paraspinal muscles of AIS. 29095406 2018