Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6913660 1.000 0.040 6 27123646 upstream gene variant C/A snv 0.14 2
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs6627057 X 145059799 downstream gene variant T/G snv 0.16 2
rs7600871
NCKAP5
2 133257389 intron variant C/T snv 0.16 2
rs802568
CNTNAP2
0.925 0.040 7 146262151 intron variant T/G snv 0.17 2
rs2524005
HLA-A
0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 3
rs10496702
NCKAP5
2 133247997 intron variant G/A snv 0.18 2
rs2044117
NALCN ; NALCN-AS1
13 101055958 intron variant G/A snv 0.19 2
rs12807809 0.882 0.160 11 124736389 upstream gene variant T/C snv 0.20 2
rs2841307 6 100308811 intergenic variant C/T snv 0.20 2
rs6484218
CAND1.11 ; AMPD3
0.882 0.040 11 10369034 intron variant G/A snv 0.21 2
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 2
rs17645023 1.000 0.040 17 66920916 intergenic variant A/T snv 0.22 2
rs12527359 6 89018502 intergenic variant T/A snv 0.23 2
rs7872515
SPTLC1
0.925 0.040 9 92060258 intron variant G/A snv 0.25 2
rs7219021
TTLL6
0.925 0.040 17 48763179 intron variant T/G snv 0.26 2
rs6932590 1.000 0.040 6 27281152 downstream gene variant T/C snv 0.26 2
rs2789588 6 72433995 intergenic variant A/C snv 0.26 1
rs2239547
ITIH4
0.882 0.040 3 52821213 intron variant T/C snv 0.27 1
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs5174
LRP8
0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 1
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 5
rs7863476
PLAA
1.000 0.040 9 26915927 intron variant G/A;C snv 0.29 2
rs4356203
PIK3C2A
0.925 0.040 11 17138601 intron variant A/G snv 0.31 3
rs7727102 5 4720472 intron variant G/C snv 0.32 2