Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1049296
rs1049296
TF
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		T 0.800 GeneticVariation GWASDB Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994

2011
dbSNP: rs10849915
rs10849915
CCDC63
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		G 0.800 GeneticVariation GWASDB Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men. 21270382

2011
dbSNP: rs12229654
rs12229654
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		G 0.800 GeneticVariation GWASDB Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men. 21270382

2011
dbSNP: rs1229984
rs1229984
ADH1B
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.800 GeneticVariation GWASDB A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. 23743675

2013
dbSNP: rs1534166
rs1534166
SRPRB
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		A 0.800 GeneticVariation GWASDB Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994

2011
dbSNP: rs1799899
rs1799899
TF
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		A 0.800 GeneticVariation GWASDB Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994

2011
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		A 0.800 GeneticVariation GWASDB Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994

2011
dbSNP: rs2072134
rs2072134
OAS3
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		A 0.800 GeneticVariation GWASDB Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men. 21270382

2011
dbSNP: rs2074356
rs2074356
HECTD4
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.800 GeneticVariation GWASDB Genome-wide testing of putative functional exonic variants in relationship with breast and prostate cancer risk in a multiethnic population. 23555315

2013
dbSNP: rs2074356
rs2074356
HECTD4
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		T 0.800 GeneticVariation GWASDB Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men. 21270382

2011
dbSNP: rs2749097
rs2749097
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		G 0.800 GeneticVariation GWASDB Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994

2011
dbSNP: rs3811647
rs3811647
TF
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		A 0.800 GeneticVariation GWASDB Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994

2011
dbSNP: rs4758317
rs4758317
LMO1 ; LOC105376536
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.800 GeneticVariation GWASDB A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. 23743675

2013
dbSNP: rs59677118
rs59677118
NFIB
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.800 GeneticVariation GWASDB A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. 23743675

2013
dbSNP: rs671
rs671
ALDH2
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.800 GeneticVariation GWASDB Genome-wide testing of putative functional exonic variants in relationship with breast and prostate cancer risk in a multiethnic population. 23555315

2013
dbSNP: rs6943555
rs6943555
AUTS2
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		A 0.800 GeneticVariation GWASDB SNP rs6943555 in autism susceptibility candidate 2 gene (AUTS2) was associated with alcohol consumption at genome-wide significance (P = 4 × 10(-8) to P = 4 × 10(-9)). 21471458

2011
dbSNP: rs10249276
rs10249276
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 GeneticVariation GWASDB ANKRD7 and CYTL1 are novel risk genes for alcohol drinking behavior. 22613542

2012
dbSNP: rs10281955
rs10281955
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 GeneticVariation GWASDB ANKRD7 and CYTL1 are novel risk genes for alcohol drinking behavior. 22613542

2012
dbSNP: rs10433415
rs10433415
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 GeneticVariation GWASDB Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994

2011
dbSNP: rs10935068
rs10935068
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 GeneticVariation GWASDB Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994

2011
dbSNP: rs10935070
rs10935070
TOPBP1
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 GeneticVariation GWASDB Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994

2011
dbSNP: rs10935073
rs10935073
TF ; INHCAP
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 GeneticVariation GWASDB Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994

2011
dbSNP: rs10953881
rs10953881
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 GeneticVariation GWASDB ANKRD7 and CYTL1 are novel risk genes for alcohol drinking behavior. 22613542

2012
dbSNP: rs10953885
rs10953885
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 GeneticVariation GWASDB ANKRD7 and CYTL1 are novel risk genes for alcohol drinking behavior. 22613542

2012
dbSNP: rs11066015
rs11066015
ACAD10
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 GeneticVariation GWASDB Genome-wide testing of putative functional exonic variants in relationship with breast and prostate cancer risk in a multiethnic population. 23555315

2013