log file:
PLINK v1.90b6.10 64-bit (17 Jun 2019)
Options in effect:
--bfile /Users/jingyuli/Desktop/PRS Group/data/Chromosome info/1kgp_chr1_nonDup
--clump /Users/jingyuli/Desktop/PRS Group/data/cvd data/nielsen-thorolfsdottir-willer-NG2018-AFib-gwas-summary-statistics-chr22-plink.txt
Hostname: lawn-128-61-120-150.lawn.gatech.edu
Working directory: /Users/jingyuli/Desktop/PRS Group/data/Chromosome info
Start time: Thu Jul 18 16:38:01 2019
Random number seed: 1563482281
16384 MB RAM detected; reserving 8192 MB for main workspace.
6467272 variants loaded from .bim file.
2504 people (0 males, 0 females, 2504 ambiguous) loaded from .fam.
Ambiguous sex IDs written to plink.nosex .
Using 1 thread (no multithreaded calculations invoked).
Before main variant filters, 2504 founders and 0 nonfounders present.
Calculating allele frequencies... done.
Total genotyping rate is 0.999841.
6467272 variants and 2504 people pass filters and QC.
Note: No phenotypes present.
Warning: No significant --clump results. Skipping.
End time: Thu Jul 18 16:38:11 2019
I have been getting the same warning message when I tried to run LD clumping in plink and I have also tested different p1, p2 values. Anyone knows how to resolve this issue?