[PMID 18187665] Identification of genetic polymorphisms associated with risk for pulmonary hypertension in sickle cell disease.

[PMID 20401335] Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.

rs2235302

Parent Gene: SELP

Importance: 3
Less common allele: T = 41%
More common allele: C = 59%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Soluble P-Selectin Measurement

The T allele of rs2235302 is reported to be associated with Soluble P-selectin Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Soluble levels of adhesion molecules (P-Selectin).