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. Author manuscript; available in PMC: 2022 Mar 1.
Published in final edited form as: Diabetologia. 2021 Dec 24;65(3):477–489. doi: 10.1007/s00125-021-05635-9

Table 2.

Significant (p<5 × 10−8) previously unreported secondary signals at known fasting insulin and fasting glucose loci

Trait Secondary Varianta Chr:Position Ref allele Alt allele Locus Effect (SE) of alt allele in conditional analysis Primary analysis transethnic p valueb Conditional analysis transethnic p valuec Primary conditioning variant(s)d LD D’e LD r2f MAF
Transethnic AA EA HA ASN HI NAm
Fasting insulin rs330941 8:9018657 C T PPP1R3B 0.045 (0.007) 4.79×10−7 2.37×10−10 rs4841132 0.18 0.005 0.43 0.29 0.39 0.49 0.22 0.27 0.43
Fasting glucose rs55908146 7:44180226 G A GCK/MYL7 0.043 (0.008) 8.03×10−6 1.75×10−8 rs2908286, rs2908290 0.04, 0.24 0.001, 0.014 0.28 0.15 0.32 0.30 0.26 0.25 0.30
a

Lead variant from conditional analysis reaching locus-specific significance

b

p value of the secondary variant in the primary GWAS analysis, not adjusted for the primary variant

c

p value of the secondary variant, adjusted for the primary variant(s)

d

Lead variant(s) from the primary analysis and previous stepwise conditional analysis

e

LD D′ between primary variant(s) and secondary variant in PAGE Study data (transethnic LD generated from unrelated subset of AA, HA, ASN, HI and NAm participants)

f

LD r2 between primary variant(s) and secondary variant in PAGE Study data (transethnic LD generated from unrelated subset of AA, HA, ASN, HI and NAm participants)