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. Author manuscript; available in PMC: 2013 Dec 1.
Published in final edited form as: Circ Cardiovasc Genet. 2012 Nov 8;5(6):639–646. doi: 10.1161/CIRCGENETICS.112.963991

Table 2.

Summary of six primary and two secondary independent loci (P < 5.0×10−8) obtained for PR in 13,415 African-American participants from ten cohort studies.

SNP Gene Chr Position
(Build 36)
Allelesa Effect allele
Frequency
Study-specific
direction of βb
β (se) p phet
Primary signalsc
rs3891585 MEIS1 2 66,610,480 A/G 0.43 +−++−+++++ 2.13 (0.31) 1.42 × 10−11 0.11
rs267567 ITGA9 3 37,549,028 A/G 0.18 +++−++++++ 2.73 (0.41) 4.14 × 10−11 0.54
rs3922844 SCN5A 3 38,599,257 T/C 0.58 −−−−−−−−−− −4.54 (0.33) 5.26 × 10−43 0.58
rs11732231 ARHGAP2
4
4 86,902,584 C/G 0.23 ++++++++++ 2.28 (0.39) 2.96 × 10−9 0.30
rs11773845 CAV1 7 115,978,537 A/C 0.36 −−−−−−−−−− −2.29 (0.33) 4.45 × 10−12 0.53
rs1895585 TBX5 12 113,286,521 A/G 0.30 ++−+++++++ 3.19 (0.35) 1.36 × 10−19 0.42
Secondary signalsd
rs6763048 SCN5A 3 38,656,398 A/G 0.73 ++++++++++ 2.62 (0.38) 3.75 × 10−12 0.74
rs6801957 SCN10A 3 38,742,319 T/C 0.27 ++++ 3.36 (0.58) 9.11 × 10−9 0.15
a

Coded allele listed first.

b

Study-specific direction of β estimates are listed in alphabetical order by study. The + and − symbols represent an increase and decrease, respectively, in the PR interval per copy of the minor allele.

c

Defined as locus-specific SNP with the lowest P-value.

d

Defined as significant SNPs after conditional analysis that adjusted for locus-specific primary signal. The conditional analysis for rs6801957 was performed in four cohorts (CHS, HABC, HANDLS and WHI) adjusting for successively less significant SNPs until no genome-wide significant SNPs remained.

Chr, chromosome; se, standard error; p, meta-analysis p-value; phet, Cochran’s Q heterogeneity p-value.