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
rs2391769
LOC105378866
0.925 0.040 1 96513405 regulatory region variant A/G;T snv 3
rs4259397 0.925 0.040 8 92354062 upstream gene variant G/A;T snv 2
rs4858253 0.925 0.040 3 20687599 intron variant C/T snv 0.33 2
rs74760947 0.925 0.040 8 34495092 intergenic variant A/G snv 3.1E-02 2
rs797267 0.925 0.040 12 89373460 intron variant A/G snv 0.28 2
rs1476535
FOXP2
0.925 0.040 7 114430980 intron variant C/G;T snv 2
rs2189012
FOXP2
0.925 0.040 7 114571857 intron variant G/A snv 0.73 2
rs56319043
KDM4A-AS1 ; ST3GAL3 ; KDM4A
0.925 0.040 1 43705540 intron variant C/T snv 0.17 2
rs4916723
LINC00461
0.925 0.040 5 88558577 intron variant A/C;G;T snv 2
rs139868495
LINC01288
0.925 0.040 8 34805452 intron variant C/T snv 3.1E-02 2
rs76545266
LOC105379365
0.925 0.040 8 34224003 upstream gene variant T/C snv 2.9E-02 2
rs145108385
LOC648987
0.925 0.040 5 43054645 intron variant A/G snv 2
rs11210887
PTPRF
0.925 0.040 1 43610348 intron variant G/A snv 0.52 2
rs2782639
PTPRF
0.925 0.040 1 43540668 intron variant A/G snv 0.26 2
rs8039398
SEMA6D
0.925 0.040 15 47438673 intron variant T/C snv 0.47 2
rs113551349
SLC6A9
0.925 0.040 1 44009451 intron variant C/T snv 0.20 2
rs12003072 1.000 9 84156246 intergenic variant C/A snv 3.2E-02 1
rs142981069 1.000 18 61158789 intergenic variant A/G snv 9.1E-03 1
rs2099149 1.000 12 30326425 downstream gene variant T/G snv 0.28 1
rs10499
ATP2A1 ; RABEP2
1.000 16 28904206 3 prime UTR variant G/A;T snv 0.70 1
rs1574587
ATP2C2
1.000 16 84419450 intron variant C/T snv 0.13 1
rs1448602
CADM2
1.000 3 85731304 intron variant A/G;T snv 0.18 1
rs2875907
CADM2
0.925 0.040 3 85469430 intron variant A/G;T snv 1
rs7651996
CADM2
1.000 3 85008198 intron variant G/A;T snv 1