Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
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
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 4
rs4327572 0.882 0.120 5 25972712 intron variant C/T snv 0.28 2
rs4765905
CACNA1C
0.827 0.040 12 2240418 intron variant G/A;C snv 2
rs7741604
CDKAL1
0.925 0.120 6 20731293 intron variant A/C;T snv 2
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 2
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 2
rs10038113 1.000 0.040 5 25902233 intergenic variant T/C snv 0.45 1
rs10058083 1.000 0.040 5 25894289 intergenic variant G/A snv 0.38 1
rs10239799 1.000 0.040 7 120765281 intergenic variant C/T snv 0.37 1
rs10513025 1.000 0.040 5 9623510 non coding transcript exon variant T/C snv 5.4E-02 1
rs10749886 1.000 0.040 11 107129809 intergenic variant G/A snv 0.35 1
rs10904487 1.000 0.040 10 5382502 intergenic variant C/T snv 0.64 1
rs11102807 1.000 0.040 1 114518963 intergenic variant A/G snv 0.44 1
rs11899372 1.000 0.040 2 127016304 upstream gene variant G/T snv 6.1E-02 1
rs12518194 1.000 0.040 5 25951452 intergenic variant A/G snv 0.27 1
rs12519594 1.000 0.040 5 25934696 intergenic variant G/A snv 0.27 1
rs12521157 1.000 0.040 5 25869292 intergenic variant C/T snv 0.28 1
rs12521388 1.000 0.040 5 25912004 downstream gene variant G/A snv 0.29 1
rs12701862 1.000 0.040 7 41083854 intergenic variant G/A snv 0.68 1
rs13166776 1.000 0.040 5 25971247 intron variant T/C snv 0.28 1
rs13176113 1.000 0.040 5 25900331 intergenic variant G/A snv 0.28 1