Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10150332
NRXN3
14 79470621 intron variant T/C snv 0.26 3
rs12967135 18 60181790 intergenic variant G/A snv 0.24 3
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 2
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 2
rs4776970
MAP2K5
15 67788548 intron variant A/T snv 0.44 2
rs806794
H2AC7 ; H3C4 ; H2BC7
6 26200449 3 prime UTR variant A/G snv 0.36 2
rs10145154
NRXN3
14 79473182 intron variant C/T snv 0.25 1
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 1
rs1440072
KCNE4
2 223072020 intron variant C/A;G;T snv 1
rs17109256
NRXN3
14 79473650 intron variant G/A snv 0.21 1
rs2075064
LHX2
9 124021568 intron variant C/T snv 0.35 1
rs2168711 18 60181298 intergenic variant T/C snv 0.24 1
rs2222328
IQCJ-SCHIP1 ; SCHIP1
3 159541502 intron variant T/C snv 0.17 1
rs2570467
LOC101929710
5 96520975 intron variant A/G snv 0.29 1
rs4471028
GDAP1
8 74382740 intron variant T/G snv 0.36 1
rs523288 18 60181136 intergenic variant A/T snv 0.27 1
rs6440003
ZBTB38
3 141375367 intron variant G/A snv 0.54 1
rs6867983
C5orf67
5 56558326 intron variant C/T snv 0.17 1
rs7601155
BABAM2
2 28124815 intron variant C/T snv 6.8E-02 1
rs7654585 4 25941129 intergenic variant A/G snv 0.60 1
rs7890572
IL1RAPL1
X 29622701 intron variant A/G snv 9.3E-02 1
rs981113
SV2C
5 76225103 intron variant T/G snv 0.62 1
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20