Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2234246
rs2234246
Entrez Id: 54210
Gene Symbol: TREM1
TREM1
CUI: C0243026
Disease:
Sepsis
0.010 GeneticVariation BEFREE Of the three tested TREM-1 SNPs (rs144672509, rs2234237, and rs2234246), only rs2234237 (Ser25Thr) was significantly associated with sepsis prognosis in three inheritance models (p < 0.05). 22798017 2012
dbSNP: rs2234237
rs2234237
Entrez Id: 54210
Gene Symbol: TREM1
TREM1
CUI: C0036690
Disease:
Septicemia
0.020 GeneticVariation BEFREE The TREM-1 rs2234237 genotype was not significantly associated with sepsis mortality and sepsis disease severity. 30832396 2019
dbSNP: rs2234237
rs2234237
Entrez Id: 54210
Gene Symbol: TREM1
TREM1
CUI: C0036690
Disease:
Septicemia
0.020 GeneticVariation BEFREE Of the three tested TREM-1 SNPs (rs144672509, rs2234237, and rs2234246), only rs223</span>4237 (Ser25Thr) was significantly associated with sepsis prognosis in three inheritance models (p < 0.05). 22798017 2012
dbSNP: rs2234246
rs2234246
Entrez Id: 54210
Gene Symbol: TREM1
TREM1
CUI: C0036690
Disease:
Septicemia
0.010 GeneticVariation BEFREE Of the three tested TREM-1 SNPs (rs144672509, rs2234237, and rs2234246), only rs2234237 (Ser25Thr) was significantly associated with sepsis prognosis in three inheritance models (p < 0.05). 22798017 2012
dbSNP: rs2234237
rs2234237
Entrez Id: 54210
Gene Symbol: TREM1
TREM1
CUI: C1719672
Disease:
Severe Sepsis
0.010 GeneticVariation BEFREE Three common polymorphisms (rs7768162, rs9471535, and rs2234237) within the TREM-1 gene were detected in 175 patients with severe sepsis and in 139 healthy control subjects. 18396215 2008
dbSNP: rs9471535
rs9471535
Entrez Id: 54210
Gene Symbol: TREM1
TREM1
CUI: C0009324
Disease:
Ulcerative Colitis
0.010 GeneticVariation BEFREE Three TREM-1 single nucleotide polymorphisms (SNPs, rs2234237, rs3789205, and rs9471535) were genotyped by Taqman technology on 202 Crohn's disease (CD), 265 ulcerative colitis (UC), 138 with intestinal Behcet's disease (BD), and 234 healthy controls and the relationships between these SNPs and IBD development and phenotypes were evaluated. 21763322 2011