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. Author manuscript; available in PMC: 2012 Jun 7.
Published in final edited form as: Hum Genet. 2011 Jul 30;131(2):275–287. doi: 10.1007/s00439-011-1071-0

Table 4.

Comparison of top association hits for analysis of a dichotomous phenotype for African Americans samples from the Multi-Ethnic Study of Atherosclerosis.

Chr SNP MAF Gene Position

(bp)
GEE:

GC 1.02
MQLS:

GC 1.0
Logistic:

GC 1.07
16 rs247617 0.26 CETP 56990716 3.8 × 10−10 2.5 × 10−8 1.2 × 10−10
12 rs10770291 0.42 RERGL 18108048 4.6 × 10−7 1.4 × 10−5 3.7 × 10−7
1 rs12407335 0.21 PRMT6 107299585 5.5 × 10−7 2.2 × 10−6 4.4 × 10−7
1 rs12409858 0.20 PRMT6 107299233 1.1 × 10−6 4.9 × 10−6 9.6 × 10−7
12 rs701069 0.16 FLJ37505 128026678 1.8 × 10−6 4.3 × 10−6 1.4 × 10−6
7 rs6974174 0.40 WIPF3 29914469 2.5 × 10−6 1.4 × 10−5 2.7 × 10−6
1 rs11184981 0.25 PRMT6 107299263 3.2 × 10−6 1.0 × 10−5 2.5 × 10−6
2 rs3940409 0.43 PARD3B 205115659 3.4 × 10−6 1.5 × 10−5 4.3 × 10−6
7 rs10251970 0.49 DYNC1I1 95596832 3.5 × 10−6 6.2 × 10−6 1.6 × 10−6
9 rs2806687 0.36 INVS 103005815 3.7 × 10−6 2.8 × 10−6 2.6 × 10−6
10 rs7086818 0.08 ANKRD30A 36893908 3.7 × 10−6 4.4 × 10−5 3.1 × 10−6
12 rs7971307 0.45 RERGL 18118930 4.2 × 10−6 5.9 × 10−5 2.7 × 10−6
10 rs7096919 0.09 ANKRD30A 36889214 4.6 × 10−6 4.2 × 10−5 2.8 × 10−6
9 rs1529191 0.32 ERP44 102845908 9.0 × 10−6 3.3 × 10−6 5.4 × 10−6
15 rs10518973 0.10 LIPC 58651580 1.8 × 10−5 1.9 × 10−6 3.1 × 10−5
2 rs13384421 0.25 NMUR1 232464308 2.0 × 10−5 2.2 × 10−6 2.7 × 10−5

Results are shown for all SNPs with p-value ≤ 5 × 10−6 by GEE or MQLS binary trait analyses, with corresponding results by logistic regression shown for comparison. GEE and logistic regression were performed with adjustment for covariates age, gender, study site, and a single principal component of ancestry, while MQLS was performed with no covariates due to a practical limitation of the method. Minor allele frequency (MAF) is shown for each SNP, and genomic control (GC) numbers are indicated for each test, with no adjustment for GC inflation in the presented association results. SNP annotation was obtained using Human Genome build 37.1 from dbSNP (http://www.ncbi.nlm.nih.gov/projects/SNP/).