Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4771122
MTIF3
1.000 0.080 13 27446043 intron variant G/A;C snv 2
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 4
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 2
rs1401635
BDNF ; BDNF-AS
0.925 0.040 11 27672444 intron variant C/G snv 0.73 2
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 2
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 3
rs867282
LOC105374378
2 27728791 regulatory region variant T/A;C snv 0.67 2
rs13013484 2 27765954 intergenic variant G/A snv 0.61 3
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 4
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 3
rs4788099
TUFM ; MIR4721
16 28844406 intron variant A/G snv 0.35 0.34 2
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs7359397
SH2B1
1.000 0.040 16 28874338 upstream gene variant C/T snv 0.28 2
rs9931989
ATP2A1
16 28894763 intron variant G/C snv 0.68 3
rs2904880
CD19 ; RABEP2
1.000 0.040 16 28933075 missense variant C/G snv 0.72 0.76 2
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 4
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 2
rs2253802
MDC1
6 30716909 5 prime UTR variant C/T snv 4.4E-02 2
rs652722
PAX6-AS1 ; PAUPAR
1.000 0.040 11 31883988 intron variant C/T snv 0.32 2
rs623312
PAUPAR ; PAX6-AS1
11 31885918 non coding transcript exon variant G/A snv 0.32 2
rs2440238
PAX6-AS1 ; PAUPAR
11 31886440 non coding transcript exon variant T/G snv 0.32 2
rs597660
PAUPAR
11 31893668 intron variant G/T snv 0.41 2