Table 2.
Gene | Location longest coding transcript |
Testd |
N variants |
P-value |
Conditioned P- valuea |
Single variant | |
---|---|---|---|---|---|---|---|
|
|||||||
Top variant | P-value | ||||||
All-ancestries sex-combined | |||||||
SLC6A17 | chr1:110693132–110744823 | SKAT | 13 | 2.73E-07 | 0.13 | rs41313405 | 4.45E-07 |
RAPGEF3 | chr12:48128453–48152889 | SKAT | 19 | 8.91E-15 | 0.20 | rs145878042 | 5.16E-14 |
PRKAG1 | chr12:49396055–49412629 | SKAT | 4 | 2.75E-12 | 0.53 | rs1126930 | 2.63E-12 |
RAB21 | chr12:72148643–72187256 | SKAT | 5 | 4.81E-08 | 0.27 | rs61754230 | 4.96E-08 |
KSR2 | chr12:117890817–118406028 | SKAT | 7 | 7.15E-09 | 0.19 | rs56214831 | 4.59E-08 |
MAP1A | chr15:43809806–43823818 | SKAT | 25 | 9.42E-07 | 0.16 | rs55707100 | 1.01E-06 |
MC4R | chr18:58038564–58040001 | VT | 4 | 3.72E-09 | 0.01 | rs13447325 | 2.97E-11 |
GIPR | chr19:46171502–46186982 | VT | 10 | 8.24E-09 | 1.12E-04 | rs143430880 | 5.76E-06 |
All-ancestries sex-specific | |||||||
ALDH3A1 (men only) | chr17:19641298–19651746 | SKAT | 15 | 3.24E-07 | 0.003 | rs142078447 | 8.62E-06 |
ZFR2 (women only) | chr19:3804022–3869027 | SKAT | 19 | 1.81E-07 | 0.82 | rs45465594 | 3.64E-07 |
European sex-combined | |||||||
ACHE | chr7:100487615–100493592 | SKAT | 6 | 3.30E-10 | 0.12 | rs386545548 | 7.22E-10 |
European sex-specific | |||||||
ANGPTL7 (men only) | chr1:11249346–11256038 | VT | 3 | 2.50E-06 | 0.008 | rs202182115 | 2.56E-05 |
ZNF169 (women only) | chr9:97021548–97064111 | SKAT | 9 | 1.89E-07 | 0.24 | rs12236219 | 1.06E-06 |
Array-wide significant gene-based association is defined as P<2.5×10−6. P-values are based on the meta-analysis of Discovery Stage studies.
Gene-based analyses were performed with SKAT and VT; results shown are from the test (SKAT or VT) for which the significance exceeded P<2.5×10−6. Only results using the "broad" SNV inclusion criteria reached array-wide significance.
Transcript positions are reported according to Build 37 for the longest coding transcript supported by RefSeq (as displayed in USCS Genome Browser).
P-value after conditioning on the most significant (top) single variant aggregated in the gene-based test.