Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17393065
rs17393065
Entrez Id: 79623
Gene Symbol: GALNT14
GALNT14
CUI: C1720994
Disease:
Eye Movement Measurements 		0.700 GeneticVariation GWASCAT Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia. 30120336 2018
dbSNP: rs6543603
rs6543603
Entrez Id: 79623
Gene Symbol: GALNT14
GALNT14
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs6760355
rs6760355
Entrez Id: 79623
Gene Symbol: GALNT14
GALNT14
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs6760355
rs6760355
Entrez Id: 79623
Gene Symbol: GALNT14
GALNT14
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs201118996
rs201118996
Entrez Id: 79623
Gene Symbol: GALNT14
GALNT14
CUI: C0455988
Disease:
Hydrops Fetalis, Non-Immune 		A 0.700 GeneticVariation CLINVAR Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families. 26036949 2015
dbSNP: rs10205350
rs10205350
Entrez Id: 79623
Gene Symbol: GALNT14
GALNT14
CUI: C0004352
Disease:
Autistic Disorder 		0.700 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504 2012
dbSNP: rs11687856
rs11687856
Entrez Id: 79623
Gene Symbol: GALNT14
GALNT14
CUI: C0027404
Disease:
Narcolepsy 		0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009
dbSNP: rs9679162
rs9679162
Entrez Id: 79623
Gene Symbol: GALNT14
GALNT14
CUI: C2239176
Disease:
Liver carcinoma 		0.060 GeneticVariation BEFREE A GALNT14 rs9679162 genotype-guided therapeutic strategy for advanced hepatocellular carcinoma: systemic or hepatic arterial infusion chemotherapy. 31611591 2020
dbSNP: rs9679162
rs9679162
Entrez Id: 79623
Gene Symbol: GALNT14
GALNT14
CUI: C2239176
Disease:
Liver carcinoma 		0.060 GeneticVariation BEFREE Combinations of single nucleotide polymorphisms WWOX-rs13338697, GALNT14-rs9679162 and rs6025211 effectively stratify outcomes of chemotherapy in advanced hepatocellular carcinoma. 28695683 2018
dbSNP: rs9679162
rs9679162
Entrez Id: 79623
Gene Symbol: GALNT14
GALNT14
CUI: C2239176
Disease:
Liver carcinoma 		0.060 GeneticVariation BEFREE The present study investigated the prognostic role of the N-acetylgalactosaminyltransferase 14 (<i>GALNT14</i>)-rs9679162 genotype, an effective therapeutic response predictor for hepatocellular carcinoma in patients with cholangiocarcinoma receiving surgical resection. 28588705 2017
dbSNP: rs9679162
rs9679162
Entrez Id: 79623
Gene Symbol: GALNT14
GALNT14
CUI: C2239176
Disease:
Liver carcinoma 		0.060 GeneticVariation BEFREE N-acetylgalactosaminyltransferase 14 (GALNT14)-rs9679162 genotype is a prognostic predictor for chemotherapy response in advanced hepatocellular carcinoma. 27124048 2016
dbSNP: rs9679162
rs9679162
Entrez Id: 79623
Gene Symbol: GALNT14
GALNT14
CUI: C2239176
Disease:
Liver carcinoma 		0.060 GeneticVariation BEFREE In conclusion, this prospective study confirmed that GALN14 genotype (rs9679162) was an effective predictor for therapeutic outcome in advanced HCC patients treated by FMP chemotherapy. 23959947 2014
dbSNP: rs9679162
rs9679162
Entrez Id: 79623
Gene Symbol: GALNT14
GALNT14
CUI: C2239176
Disease:
Liver carcinoma 		0.060 GeneticVariation BEFREE The rs9679162 GALNT14 genotype is potentially associated with the objective response of the first course of FMP chemotherapy in patients with far advanced hepatocellular carcinoma. 21635146 2011
dbSNP: rs9679162
rs9679162
Entrez Id: 79623
Gene Symbol: GALNT14
GALNT14
CUI: C0686619
Disease:
Secondary malignant neoplasm of lymph node 		0.010 GeneticVariation BEFREE In conclusion, the G<i>ALNT14</i>-rs9679162 'TT' genotype was associated with perineural invasion and lymph node metastasis, as well as unfavorable overall survival in patients with resected cholangiocarcinoma. 28588705 2017
dbSNP: rs9679162
rs9679162
Entrez Id: 79623
Gene Symbol: GALNT14
GALNT14
CUI: C1269955
Disease:
Tumor Cell Invasion 		0.010 GeneticVariation BEFREE In conclusion, the G<i>ALNT14</i>-rs9679162 'TT' genotype was associated with perineural invasion and lymph node metastasis, as well as unfavorable overall survival in patients with resected cholangiocarcinoma. 28588705 2017
dbSNP: rs9679162
rs9679162
Entrez Id: 79623
Gene Symbol: GALNT14
GALNT14
CUI: C0206698
Disease:
Cholangiocarcinoma 		0.010 GeneticVariation BEFREE In conclusion, the G<i>ALNT14</i>-rs9679162 'TT' genotype was associated with perineural invasion and lymph node metastasis, as well as unfavorable overall survival in patients with resected cholangiocarcinoma. 28588705 2017