TUBA3C, tubulin alpha 3c, 7278

N. diseases: 8; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17076896
rs17076896
Entrez Id: 7278;101928697
Gene Symbol: TUBA3C;LOC101928697
TUBA3C;LOC101928697
CUI: C0026691
Disease:
Mucocutaneous Lymph Node Syndrome 		G 0.710 GeneticVariation GWASCAT Upon our previous genotyping data of 157 valid KD subjects, a genome-wide association study (GWAS) has been conducted among 11 (7%) CAA-developed KD patients to reveal five significant genetic variants passed pre-defined thresholds and resulted in two novel susceptibility protein-coding genes, which are NEBL (rs16921209 (P = 7.44 × 10(-9); OR = 32.22) and rs7922552 (P = 8.43 × 10(-9); OR = 32.0)) and TUBA3C (rs17076896 (P = 8.04 × 10(-9); OR = 21.03)). 27171184 2016
dbSNP: rs17076896
rs17076896
Entrez Id: 7278;101928697
Gene Symbol: TUBA3C;LOC101928697
TUBA3C;LOC101928697
CUI: C0026691
Disease:
Mucocutaneous Lymph Node Syndrome 		0.710 GeneticVariation BEFREE Upon our previous genotyping data of 157 valid KD subjects, a genome-wide association study (GWAS) has been conducted among 11 (7%) CAA-developed KD patients to reveal five significant genetic variants passed pre-defined thresholds and resulted in two novel susceptibility protein-coding genes, which are NEBL (rs16921209 (P = 7.44 × 10(-9); OR = 32.22) and rs7922552 (P = 8.43 × 10(-9); OR = 32.0)) and TUBA3C (rs17076896 (P = 8.04 × 10(-9); OR = 21.03)). 27171184 2016
dbSNP: rs17076896
rs17076896
Entrez Id: 7278;101928697
Gene Symbol: TUBA3C;LOC101928697
TUBA3C;LOC101928697
CUI: C0010051
Disease:
Coronary Aneurysm 		G 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Identifies Novel Susceptibility Genes Associated with Coronary Artery Aneurysm Formation in Kawasaki Disease. 27171184 2016
dbSNP: rs17076896
rs17076896
Entrez Id: 7278;101928697
Gene Symbol: TUBA3C;LOC101928697
TUBA3C;LOC101928697
CUI: C1842937
Disease:
AURAL ATRESIA, CONGENITAL 		0.010 GeneticVariation BEFREE Upon our previous genotyping data of 157 valid KD subjects, a genome-wide association study (GWAS) has been conducted among 11 (7%) CAA-developed KD patients to reveal five significant genetic variants passed pre-defined thresholds and resulted in two novel susceptibility protein-coding genes, which are NEBL (rs16921209 (P = 7.44 × 10(-9); OR = 32.22) and rs7922552 (P = 8.43 × 10(-9); OR = 32.0)) and TUBA3C (rs17076896 (P = 8.04 × 10(-9); OR = 21.03)). 27171184 2016