rs1805192 is a SNP of the PPARG gene. It is significantly associated with hypertriglyceridemia [R1, R2].

The minor allele was associated with a lower essential hypertension (EH) (OR=0.65) [R].

The carriers of the ''C'' allele showed a decreased diabetic retinopathy (DR) risk (OR=0.86) [R].

rs1805192

Parent Gene: PPARG

Importance: 2
Less common allele: G = None
More common allele: C = None
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