Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 6
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs2251219
SMIM4 ; PBRM1
0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 3
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 2
rs7225002
KANSL1
0.925 0.080 17 46111701 intron variant A/G snv 0.39 2
rs199505
WNT3 ; LRRC37A2
0.925 0.120 17 46782044 intron variant A/G snv 0.84 2
rs7713917 0.925 0.040 5 79533426 upstream gene variant A/G snv 0.54 1
rs8007267 0.882 0.200 14 54912273 intergenic variant C/T snv 0.31 1
rs1789891
ADH1B
1.000 0.080 4 99329262 intron variant C/A snv 0.13 1
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 1
rs841
GCH1
0.827 0.200 14 54843774 splice region variant G/A snv 0.22 0.22 1
rs9303521
LINC02210-CRHR1
0.925 0.120 17 45727828 intron variant T/C;G snv 0.60 1
rs2435200
MAPT
0.925 0.080 17 45994485 intron variant G/A snv 0.40 1
rs754593
MAPT
1.000 0.040 17 45977330 non coding transcript exon variant G/A snv 0.52 1
rs8067056
MAPT
0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 1
rs2522833
PCLO
0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 1
rs717454
REV1
1.000 0.040 2 99406310 non coding transcript exon variant T/C;G snv 0.44; 8.2E-06 1
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1