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. Author manuscript; available in PMC: 2016 May 1.
Published in final edited form as: Mol Psychiatry. 2014 Oct 7;20(5):647–656. doi: 10.1038/mp.2014.107

Table 3.

Associations between coffee consumption loci and other traits

Lead SNP,
allele ↑ coffee
consumptiona
closest gene
Other Traitsb
higher levels/riskc lower levels/riskc
rs1260326, C
GCKR
non-albumin protein
fasting glucose
HOMA-IR
fasting insulin
mannose
serum albumin
2-hr glucose challenge
metabolic syndrome
glucose/mannose ratio
total cholesterol
triglycerides
hypertriglyceridemia
chronic kidney disease
uric acid
SHBG Crohn’s disease
C-reactive protein
platelet counts
GGT docosapentaenoic acid
alanine/glutamine ratio
alanine
LDL (P=2.33×10−4)
waist-to-hip-ratio (P=3.40×10−4)
bipolar disorder (P=2.31×l0−3)
rs1481012, A
ABCG2
LDL response to statins (‘responders’)
uric acid
body mass index (P=4.85×10−3)
rs6968554 , G
AHR
caffeine
HDL (P=1.18×10−3)
rs7800944, C
MLXIPL
triglycerides
HDL (P=2.24×10−3)
birth weight (P=2.10×10−3)
rs6265, C
BDNF
smoking initiation
body mass index
DBP (P=6.58×10−4)
rs2472297d, T
CYP1A1_CYP1A2
caffeine e
SBP (P=6.81×10−5)
DBP (P=6.75×10−6)
rs9902453,G
EFCAB5
SBP (P=6.05×10−3)

Abbreviations: DBP, diastolic blood pressure; GGT, gamma-glutamyltransferase; HDL, high density lipoprotein; LDL, low density lipoprotein; SBP, systolic blood pressure; SHBG, sex hormone binding globulin

a

Lead SNP-allele associated with higher coffee consumption.

b

Traits associated with lead SNP (or close proxies: r2>0.80) according to previous GWAS20(Shin et al, 2014). Grey cells denote all GW-significant significant associations (P<5.00 ×l0−8 20 or P<1.03 ×l0−10 (Shin et al, 2014) and white cells denote coffee-relevant trait associations (P<;6.25×l0−3). See Supplementary Information for details and references to original GWAS.

c

Relative to allele associated with higher coffee consumption.

d

rsl378942 A, also associated with higher coffee consumption (P< 1.46×10−17) in stage 1 of the current report but in low LD with rs2472297 (CEU: r2=0.10), was previously associated with lower DBP in GWAS (P<5,00× 10−8).

e

Borderline significant (P<1.51 ×10−10) according to Shin et al21.