Skip to main content
. 2021 May 20;11:301. doi: 10.1038/s41398-021-01407-6

Table 2.

Distribution of allele frequency and P value of top four SNPs significantly associated with early-onset BPI disorder (≤20 years of age) in discovery and replication groups.

SNP ID CHR BPa Gene/Feature Allele Group Minor allele frequency (%) P OR (95% CI) Pmeta(SAS)/
Pmeta(PLINK)
≤20 >20
rs75928006 19 54254388 MIR522/upstream C/T Discovery 9.4 3.9 6.45 × 10−9 2.58 (1.86, 3.60)

9.23 × 10–8/

8.14 × 10−5

Replication 15.7 16.7 0.7084 0.93 (0.64, 1.34)
rs11127876 3 85124697 CADM2/intronic C/T Discovery 9.3 4.1 7.04 × 10−8 2.39 (1.73, 3.31)

5.19 × 10−8/

1.26 × 10−7

Replication 21.2 15.6 0.0354 1.46 (1.03, 2.06)
rs7914868 10 16973722 CUBN/intronic C/G Discovery 12.4 6.3 7.59 × 10−8 2.10 (1.59, 2.76)

7.00 × 10−7/

8.31 × 10−6

Replication 24.5 22.5 0.5102 1.12 (0.81, 1.54)
rs10106565 8 8855032 MFHAS1-ERI1/intergenic C/T Discovery 9.8 4.5 9.70 × 10−8 2.31 (1.68, 3.16)

1.33 × 10−7/

4.38 × 10−5

Replication 18.6 17.8 0.7866 1.06 (0.74, 1.50)

P values, ORs, and CIs were calculated based on the allele model.

OR odds ratio, CI confidence interval, Pmeta (SAS), Pmeta (PLINK) P value of meta-analysis generated by SAS and PLINK v. 1.9 program.

aLocation was cited according to GRCh37.p13.