Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 6
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 4
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 4
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 3
rs578776
CHRNA3
0.742 0.240 15 78596058 3 prime UTR variant G/A snv 0.39 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 3
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 2
rs10994397
ANK3
0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 2
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40 2
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 2
rs498793
FADS2
1.000 0.040 11 61857233 intron variant T/C snv 0.62 2
rs548181
FEZ1 ; STT3A-AS1 ; STT3A
0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 2
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 2
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 2
rs7004633
LOC105375630
0.851 0.040 8 88748082 intron variant A/G snv 0.28 2
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 2
rs17662626
LOC107985969
0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 2
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 2
rs206936
RPS10-NUDT3 ; NUDT3
0.882 0.160 6 34335092 intron variant A/G snv 0.34 2
rs12576775
TENM4
0.827 0.080 11 79366149 intron variant A/G snv 0.15 2