ABI3, ABI family member 3, 51225

N. diseases: 27; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs850526
rs850526
Entrez Id: 2793;51225
Gene Symbol: GNGT2;ABI3
GNGT2;ABI3
CUI: C0008313
Disease:
Cholangitis, Sclerosing
C 0.700 GeneticVariation GWASCAT Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease. 27992413 2017
dbSNP: rs616338
rs616338
Entrez Id: 51225
Gene Symbol: ABI3
ABI3
CUI: C0002395
Disease:
Alzheimer's Disease
0.020 GeneticVariation BEFREE Using Fisher's exact test, there was significant association of both ABI3_rs616338-T (OR = 1.41, p = 0.044) and PLCG2_rs72824905-G (OR = 0.56, p = 0.008) with AD. 30326945 2018
dbSNP: rs616338
rs616338
Entrez Id: 51225
Gene Symbol: ABI3
ABI3
CUI: C0002395
Disease:
Alzheimer's Disease
0.020 GeneticVariation BEFREE We observed three new genome-wide significant nonsynonymous variants associated with Alzheimer's disease: a protective variant in PLCG2 (rs72824905: p.Pro522Arg, P = 5.38 × 10<sup>-10</sup>, odds ratio (OR) = 0.68, minor allele frequency (MAF)<sub>cases</sub> = 0.0059, MAF<sub>controls</sub> = 0.0093), a risk variant in ABI3 (rs616338: p.Ser209Phe, P = 4.56 × 10<sup>-10</sup>, OR = 1.43, MAF<sub>cases</sub> = 0.011, MAF<sub>controls</sub> = 0.008), and a new genome-wide significant variant in TREM2 (rs143332484: p.Arg62His, P = 1.55 × 10<sup>-14</sup>, OR = 1.67, MAF<sub>cases</sub> = 0.0143, MAF<sub>controls</sub> = 0.0089), a known susceptibility gene for Alzheimer's disease. 28714976 2017
dbSNP: rs16947151
rs16947151
Entrez Id: 51225
Gene Symbol: ABI3
ABI3
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE We found that, in the progressive mild cognitive impairment group, rs5978930 was associated with total tau levels and rs16947151 was associated with cognitive function scores at baseline and over time, suggesting that ABI3 variants may be associated with cognitive decline and may influence AD onset through tau pathology. 31127786 2019
dbSNP: rs16947151
rs16947151
Entrez Id: 51225
Gene Symbol: ABI3
ABI3
CUI: C1270972
Disease:
Mild cognitive disorder
0.010 GeneticVariation BEFREE We found that, in the progressive mild cognitive impairment group, rs5978930 was associated with total tau levels and rs16947151 was associated with cognitive function scores at baseline and over time, suggesting that ABI3 variants may be associated with cognitive decline and may influence AD onset through tau pathology. 31127786 2019
dbSNP: rs16947151
rs16947151
Entrez Id: 51225
Gene Symbol: ABI3
ABI3
CUI: C0338656
Disease:
Impaired cognition
0.010 GeneticVariation BEFREE We found that, in the progressive mild cognitive impairment group, rs5978930 was associated with total tau levels and rs16947151 was associated with cognitive function scores at baseline and over time, suggesting that ABI3 variants may be associated with cognitive decline and may influence AD onset through tau pathology. 31127786 2019
dbSNP: rs16947151
rs16947151
Entrez Id: 51225
Gene Symbol: ABI3
ABI3
CUI: C0234985
Disease:
Mental deterioration
0.010 GeneticVariation BEFREE We found that, in the progressive mild cognitive impairment group, rs5978930 was associated with total tau levels and rs16947151 was associated with cognitive function scores at baseline and over time, suggesting that ABI3 variants may be associated with cognitive decline and may influence AD onset through tau pathology. 31127786 2019
dbSNP: rs616338
rs616338
Entrez Id: 51225
Gene Symbol: ABI3
ABI3
CUI: C0752347
Disease:
Lewy Body Disease
0.010 GeneticVariation BEFREE None of the other cohorts showed significant associations that were concordant with those for AD, although the DLB cohort had suggestive findings (Fisher's test: ABI3_rs616338-T OR = 1.79, p = 0.097; PLCG2_rs72824905-G OR = 0.32, p = 0.124). 30326945 2018