INKA2, inka box actin regulator 2, 55924

N. diseases: 7; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1546924
rs1546924
Entrez Id: 55924
Gene Symbol: INKA2
INKA2
CUI: C1305855
Disease:
Body mass index 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs2076586
rs2076586
Entrez Id: 55924
Gene Symbol: INKA2
INKA2
CUI: C0205682
Disease:
Waist-Hip Ratio 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs488200
rs488200
Entrez Id: 55924
Gene Symbol: INKA2
INKA2
CUI: C0010346
Disease:
Crohn Disease 		T 0.700 GeneticVariation GWASCAT A Genome-wide Association Study Identifying RAP1A as a Novel Susceptibility Gene for Crohn's Disease in Japanese Individuals. 30500874 2019
dbSNP: rs6658723
rs6658723
Entrez Id: 55924
Gene Symbol: INKA2
INKA2
CUI: C0205682
Disease:
Waist-Hip Ratio 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs12038204
rs12038204
Entrez Id: 5906;55924
Gene Symbol: RAP1A;INKA2
RAP1A;INKA2
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs488200
rs488200
Entrez Id: 55924
Gene Symbol: INKA2
INKA2
CUI: C0018553
Disease:
Hamartoma Syndrome, Multiple 		0.010 GeneticVariation BEFREE Transcriptome analysis of CD4+ effector memory T cells from lamina propria mononuclear cells of CD patients revealed a significant association of rs488200 with RAP1A expression. 30500874 2019
dbSNP: rs197388
rs197388
Entrez Id: 11218;55924;101928718
Gene Symbol: DDX20;INKA2;LOC101928718
DDX20;INKA2;LOC101928718
CUI: C0017601
Disease:
Glaucoma 		0.010 GeneticVariation BEFREE The correlation between the data and clinical parameters has shown that the A allele of rs197388 in relation to retinal nerve fiber layer(RNFL) could be responsible for an increased risk of glaucoma occurrence (P = 0.028), while the AT genotype could be associated with a decreased risk of POAG according to the mean deviation parameter (P = 0.023). 29095070 2018
dbSNP: rs197388
rs197388
Entrez Id: 11218;55924;101928718
Gene Symbol: DDX20;INKA2;LOC101928718
DDX20;INKA2;LOC101928718
CUI: C0339573
Disease:
Glaucoma, Primary Open Angle 		0.010 GeneticVariation BEFREE Our data has shown that GEMIN3 gene (rs197388) polymorphisms might be associated with a risk of POAG development in the Polish population. 29095070 2018
dbSNP: rs6573
rs6573
Entrez Id: 5906;55924
Gene Symbol: RAP1A;INKA2
RAP1A;INKA2
CUI: C0279626
Disease:
Squamous cell carcinoma of esophagus 		0.010 GeneticVariation BEFREE Our study highlights RAP1A and SNP rs6573 functioning as potential personal diagnostic and prognosis markers for ESCC. 22859270 2012