Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 2
rs9651118
MTHFR
0.683 0.480 1 11802157 intron variant T/C snv 0.18 2
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 1
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 5
rs1065852
NDUFA6-DT ; LOC112268294 ; CYP2D6
0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 2
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 5
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 6
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 5
rs419598
IL1RN
0.742 0.280 2 113129630 synonymous variant T/C snv 0.26 0.21 1
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 3
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 1
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 1
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 1
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 7
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 5
rs11868035
RAI1 ; SREBF1
0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 1
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 4
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 3
rs10828317
PIP4K2A
0.776 0.280 10 22550699 missense variant T/C snv 1
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 1
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8