PIP, prolactin induced protein, 5304

N. diseases: 109; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9986765
rs9986765
Entrez Id: 5304
Gene Symbol: PIP
PIP
CUI: C0011633
Disease:
Dermatomyositis
0.710 GeneticVariation BEFREE We investigated whether the three SNP (rs7750458, rs9501251 and rs9500928) at 6p21.32 in the HLA-DPB1 gene were significantly associated with DM (P < 5 × 10<sup>-8</sup> ) and identified two susceptibility loci at 7q34 (PIP, rs9986765, P = 7.45 × 10<sup>-7</sup> , odds ratio [OR] = 2.71) and 10q24.2 (CPN1, rs3750716, P = 9.04 × 10<sup>-7</sup> , OR = 4.39) with suggestive evidence. 27153935 2016
dbSNP: rs9986765
rs9986765
Entrez Id: 5304
Gene Symbol: PIP
PIP
CUI: C0011633
Disease:
Dermatomyositis
G 0.710 GeneticVariation GWASCAT Variation at HLA-DPB1 is associated with dermatomyositis in Chinese population. 27153935 2016