Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 5
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 6
rs3736228
LRP5
0.752 0.400 11 68433827 missense variant C/T snv 0.13 0.11 1
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 7
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 5
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs9357271
BTBD9
0.776 0.160 6 38398097 intron variant T/C snv 0.38 1
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 6
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 6
rs3743078
CHRNA3
0.807 0.160 15 78602417 intron variant C/A;G snv 1
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 10
rs12576775
TENM4
0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 5
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 5
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 5
rs3749034
GAD1
0.827 0.040 2 170816965 5 prime UTR variant G/A;T snv 1
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs10994397
ANK3
0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 5
rs11152369
TCF4
0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs12325410
LOC101927026
0.851 0.040 16 9581389 intron variant T/G snv 0.16 5