Table 2

Association results for lead markers of regions entering the validation stage of the primary and sensitivity GWAS analysis

Lead
SNPs
LocusChrSNP IDEA,
ED
Discovery (stage 1)Replication (stage 2)Eff.
Dir.
I2pheterog.Combined (stage 1 & 2)‡
P value*OR (95% CI)EAF
Ca|Co|Eur
Meta
P value+*
OR (95% CI)Meta P value+*OR(95% CI)I2
GWAS analysis 1 (pc adjusted)*
SNP 1PNPLA3§22rs2294915T+6.21×10−151.71 (1.50 to 1.96).49|.36|.246.19×10-61.89 (1.44 to 2.50)+++00.5172.44×10−191.75 (1.55 to 1.97)0
PNPLA322rs738409G+7.23×10−151.71 (1.49 to 1.96).48|.35|.229.74×10-61.89 (1.42 to 2.50)+++00.5784.31×10−191.74 (1.54 to 1.97)0
SNP 2TM6SF2¶19rs58489806T+1.42×10−91.87 (1.53 to 2.29).17|.10|.085.22×10-41.91 (1.33 to 2.76)++−540.1103.04×10−121.88 (1.57 to 2.25)32
TM6SF219rs58542926T+2.81×10−91.94 (1.56 to 2.42).15|.08|.077.58×10-52.11 (1.46 to 3.04)++−610.0761.00×10−121.98 (1.64 to 2.40)43
SNP 3TERT5rs2242652A-7.87×10−70.64 (0.53 to 0.76).13|.19|.191.07×10-30.48 (0.31 to 0.74)−−−00.8146.40×10−90.61 (0.52 to 0.72)0
SNP 4LINC0093912rs12371263A-9.59×10−70.63 (0.52 to 0.76).16|.21|.200.3320.83 (0.57 to 1.21)−+−00.535
SNP 5DMAC219rs17318596A-2.49×10−60.71 (0.61 to 0.82).33|.40|.370.8491.03 (0.77 to 1.38)−+−150.308
SNP 6SP1002rs6743289C-2.77×10−60.72 (0.62 to 0.82).45|.52|.470.0460.75 (0.57 to 1.00)−−−00.936
SNP 7GPIHBP18rs118088203T-3.60×10−60.24 (0.13 to 0.44).01|.03|.020.2291.64 (0.73 to 3.07)+++00.697
SNP 8CNPY17rs12698003T+3.65×10−61.39 (1.21 to 1.60).46|.39|.410.0530.74 (0.55 to 1.00)−−−410.179
SNP 9GLYR116rs741692T+4.16×10−61.58 (1.30 to 1.92).18|.12|.150.7831.05 (0.73 to 1.51)++−00.541
GWAS analysis 2 (pc, sex, age adjusted)†
SNP 1PNPLA3§22rs2294915T+6.31×10−141.76 (1.52 to 2.05).49|.36|.243.24×10-51.89 (1.40 to 2.54)+++00.4281.06×10-171.79 (1.57 to 2.04)0
PNPLA322rs738409G+1.67×10−131.75 (1.51 to 2.03).48|.35|.224.17×10-51.85 (1.37 to 2.50)+++00.4485.35×10-171.77 (1.55 to 2.02)0
SNP 2TM6SF2¶19rs143988316T+4.40×10−81.91 (1.51 to 2.41).16|.09|.075.17×10-21.54 (1.00 to 2.38)++−00.6219.14×10-91.81 (1.51 to 2.16)0
TM6SF219rs58542926T+1.21×10−71.93 (1.51 to 2.45).15|.08|.071.56×10-42.16 (1.45 to 3.22)++−480.1498.80×10-111.99 (1.61 to 2.44)26
SNP 3SCN5A3rs6599222C+2.86×10−61.53 (1.28 to 1.84).25|.20|.210.9771.01 (0.68 to 1.48)−++00.984
SNP 4intergenic13rs148892410A-3.77×10−60.16 (0.07 to 0.35).01|.02|.010.7981.45 (0.09 to 24.2)++−170.299
SNP 5intergenic2rs6739777G-5.03×10−60.69 (0.59 to 0.81).29|.34|.300.3880.86 (0.61 to 1.21)−+−400.193
SNP 6ENSG0000026915119rs143660337A-5.14×10−60.41 (0.28 to 0.60).03|.05|.040.1511.68 (0.83 to 3.41)++−00.589
SNP 7LOC1053743083rs58339845T-5.84×10−60.46 (0.33 to 0.65).05|.07|.070.3611.34 (0.72 to 2.50)+++00.919
SNP 8intergenic7rs16869539G+5.96×10−61.48 (1.25 to 1.75).36|.30|.370.5370.90 (0.65 to 1.25)−−−00.983
SNP 9CELF210rs2277212T+6.84×10−61.57 (1.29 to 1.91).75|.70|.740.2821.22 (0.85 to 1.74)+−+160.303
SNP 10intergenic7rs6462611C+7.82×10−61.41 (1.21 to 1.64).49|.44|.500.0170.68 (0.49 to 0.93)++−00.465
SNP 11ENSG0000022775721rs2017196T+8.73×10−61.70 (1.34 to 2.14).89|.85|.880.0920.68 (0.44 to 1.06)−−−00.513
SNP 12TERT5rs2242652A-9.28×10−60.64 (0.52 to 0.78).13|.19|.192.60×10-40.41 (0.25 to 0.66)++−00.6994.08×10-80.60 (0.50 to 0.72)17
SNP 13RARB3rs7617311A+9.32×10−61.50 (1.25 to 1.80).28|.21|.260.4540.87 (0.61 to 1.25)−+−00.751
SNP 14CIAO2A15rs2922508T+9.53×10−61.61 (1.30 to 1.99).17|.13|.150.1531.33 (0.90 to 1.97)+++00.797
SNP 15intergenic2rs56209271T-9.67×10−60.69 (0.59 to 0.82).28|.34|.300.1680.78 (0.55 to 1.11)−−−610.075
  • *OR and p value adjusted for top 15 PCs of genetic ancestry.

  • †OR and p value adjusted for sex, age and top 15 PCs of genetic ancestry.

  • ‡The results of the combined analyses are only provided for variants meeting a Bonferroni corrected p<0.05 at the replication stage (printed in bold face).

  • §The tag SNP rs2294915 in PNPLA3 is in LD (r2= 0.92) with the functional variant rs738409 previously reported at the PNPLA3 locus58 59.

  • ¶The intergenic tag SNP rs143988316 is in strong LD (r2= 0.88) with the functional variant rs58542926 previously reported at the TM6SF2 locus.60

  • +, Significance derived from a fixed effect meta-analysis; Ca, Cases (Cirrhosis with HCC); Chr, chromosome; Co, Controls (Cirrhosis without HCC); EA, effect allele; EAF, allele frequency of the effect allele; ED, effect direction; HCC, hepatocellular carcinoma; I2, percentage of between cohort heterogeneity; LD, linkage disequilibrium; pheterog, heterogeneity p value of the meta-analysis; SNP, single-nucleotide polymorphism.