Table 2.
Hit Number | Marker Name | Chromosome | Position | Closest Reference Gene | Distance (bp) From Closest Gene or Function | Alleles |
Study Effect Direction | Number of Supporting SNPs | Effective Sample Size (proportion of total) | Second Discovery Stage Meta-analysis–CHARGE Plus Leiden and Denmark Cohorts |
||||||
Minor | Major | MAF | OR | p Value | Study Effect Direction Leiden/Denmark | OR | p Value | |||||||||
1 | rs4443878 | 1 | 238971041 | RGS7 | 34,398 | T | C | .04 | 0.41 | 1.3 × 10−6 | −−−− | 10 | 2,435 | ++ | 0.83 | .068 |
2 | rs9825185 | 3 | 196415923 | C3orf21 | Intron | C | A | .13 | 1.44 | 2.5 × 10−6 | ++++ | 24 | 0.64 | −− | 1.10 | .045 |
3 | rs954551 | 6 | 102886028 | GRIK2 | 262,554 | G | A | .25 | 0.77 | 5.3 × 10−6 | −−−− | 55 | 0.88 | † | — | — |
4 | rs7624691 | 3 | 138345769 | IL20RB | 133,159 | C | T | .43 | 0.80 | 8.8 × 10−6 | −−−− | 67 | 0.92 | ++ | 0.95 | .092 |
5 | rs10888267 | 1 | 246126046 | OR2W3 | Missense | C | T | .45 | 1.25 | 9.7 × 10−6 | ++++ | 2 | 0.92 | † | — | — |
6 | rs9972933 | 17 | 28589381 | ACCN1 | Intron | T | C | .23 | 0.77 | 1.1 × 10−5 | −−−− | 30 | 0.91 | +− | 0.89 | .003 |
7 | rs2739532 | 4 | 190944424 | C | G | .27 | 1.48 | 1.1 × 10−5 | ?+?+ | 9 | 0.99 | ‡ | — | — | ||
8 | rs8029244 | 15 | 98826098 | LASS3 | Intron | A | G | .49 | 0.79 | 1.2 × 10−5 | −−−− | 108 | 0.37 | +− | 0.90 | .002 |
9 | rs16850255 | 1 | 175085164 | PAPPA2 | 6,573 | C | T | .21 | 0.75 | 1.2 × 10−5 | −−−− | 81 | 0.86 | ++ | 0.92 | .041 |
10 | rs1543505 | 14 | 22432468 | REM2 | 5,739 | G | A | .28 | 1.27 | 1.3 × 10−5 | ++++ | 23 | 0.83 | −+ | 1.12 | .001 |
11 | rs7321904 | 13 | 80681190 | SPRY2 | 868,103 | T | C | .07 | 0.64 | 1.3 × 10−5 | −−−− | 40 | 0.93 | ++ | 0.92 | .179 |
12 | rs17401847 | 1 | 20111053 | OTUD3 | 971 | G | A | .15 | 1.38 | 1.4 × 10−5 | ++++ | 26 | 0.90 | −+ | 1.12 | .015 |
13 | rs3124736 | 10 | 115487102 | CASP7 | 6,450 | A | G | .03 | 2.30 | 1.4 × 10−5 | +++? | 0 | 0.89 | ‡ | — | — |
14 | rs690232 | 9 | 92422258 | DIRAS2 | Intron | A | G | .30 | 1.27 | 1.6 × 10−5 | +++− | 68 | 0.64 | † | — | — |
15 | rs9664222 | 10 | 89328613 | MINPP1 | 25,489 | A | C | .21 | 0.77 | 1.6 × 10−5 | −−−− | 55 | 0.93 | −− | 0.82 | 6.77 × 10−7 |
16 | rs11157721 | 14 | 49586464 | LOC196913 | 33,655 | T | C | .39 | 0.79 | 1.7 × 10−5 | −−−− | 53 | 0.86 | +− | 0.90 | .002 |
17 | rs4690810 | 4 | 166500130 | SC4MOL | 16,456 | C | T | .35 | 0.79 | 1.9 × 10−5 | −−−− | 81 | 0.85 | ++ | 0.93 | .044 |
18 | rs11605096 | 11 | 113047320 | TMPRSS5 | 16,162 | A | C | .12 | 0.71 | 1.9 × 10−5 | −−−− | 94 | 0.93 | † | — | — |
19 | rs16972414 | 18 | 35709920 | PIK3C3 | 2,079,276 | G | A | .30 | 0.79 | 2.0 × 10−5 | −−−− | 94 | 0.93 | † | — | — |
20 | rs12935091 | 16 | 70082709 | ZNF19 | 1,954 | G | A | .07 | 0.62 | 2.0 × 10−5 | −−−− | 46 | 0.94 | −+ | 0.80 | .002 |
21 | rs210332 | 14 | 53262222 | BMP4 | 223,982 | C | T | .19 | 1.33 | 2.3 × 10−5 | ++++ | 2 | 0.65 | † | — | — |
22 | rs17369174 | 8 | 76128602 | CRISPLD1 | 19,256 | G | T | .10 | 0.69 | 2.3 × 10−5 | −−−− | 83 | 0.79 | +− | 0.86 | .014 |
23 | rs6721003 | 2 | 166931758 | SCN7A | 38,026 | A | G | .45 | 1.23 | 2.4 × 10−5 | ++++ | 55 | 0.91 | −+ | 1.09 | .006 |
24 | rs4734457 | 8 | 101573533 | ANKRD46 | 28,644 | A | C | .10 | 1.75 | 2.5 × 10−5 | ++++ | 0 | 0.99 | +− | 1.10 | .098 |
Notes: p Values are for the inverse variance–weighted meta-analysis. Distances to genes are given in base pairs. Position is for NCBI Build 36. ORs are for each additional minor allele. Number of supporting SNPs: The number of SNPs within 500 kb of the top SNP that are in LD with the top SNP in the HapMap CEU release 22 (r2 ≥ .10) and have association p < .05. For imputed and direction, study-specific information is presented in the order: Age, Gene/Environment Susceptibility-Reykjavik Study, Rotterdam Study, FHS, CHS, Leiden, and Denmark. Direction: + = minor allele increases odds of survival more than 90; − = minor allele decreases odds of survival; ? = not tested. CEU = Centre d'Etude du Polymorphisme Humain European Ancestry; CHARGE = Cohorts for Heart and Aging Research in Genomic Epidemiology; CHS = Cardiovascular Health Study; FHS = Framingham Heart Study; LD = linkage disequilibrium; MAF = minor allele frequency; OR = odds ratio; SNPs = single-nucleotide polymorphisms.
For information on all SNP associations with p < 10−4, see Supplementary Table 2.
Genotyping requested, not completed.
Genotyping not requested.