Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001007
CCR5AS
0.827 0.120 3 46387167 intron variant A/G;T snv 5
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 2
rs1004234
LINC02863 ; IRF1-AS1
0.827 0.120 5 132421409 intron variant A/G;T snv 5
rs1008953 1.000 0.040 20 45352086 upstream gene variant T/C snv 0.79 1
rs10094579 0.807 0.280 8 89837077 downstream gene variant C/A snv 0.18 5
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 1
rs1047781
LOC105447645 ; FUT2
0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 2
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 2
rs10510607
CMC1
0.827 0.120 3 28244770 intron variant C/T snv 0.15 5
rs10515778
LINC01932
1.000 0.040 5 159231004 intron variant A/G snv 0.13 1
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 1
rs1051738
PDE4A
1.000 0.040 19 10467167 missense variant C/A;T snv 0.17; 4.8E-05 1
rs1056198
RNF114
0.925 0.040 20 49939692 intron variant C/T snv 0.34 2
rs10743181 0.827 0.120 11 2208529 regulatory region variant A/G snv 0.77 5
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs10750899 0.827 0.120 11 58517478 intergenic variant G/A snv 0.95 5
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 1
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 6
rs10761648
ZNF365
0.827 0.120 10 62594503 intron variant C/T snv 0.20 5
rs10775412
KSR1
0.827 0.120 17 27542007 intron variant A/C snv 0.30 5
rs10782001
FBXL19
1.000 0.040 16 30931304 intron variant G/A snv 0.53 1
rs10789285 1.000 0.040 1 69322799 intergenic variant T/G snv 0.33 2
rs10794648 1.000 0.040 1 24191716 upstream gene variant T/C snv 0.68 1
rs10800314 0.827 0.120 1 161502999 upstream gene variant C/A snv 0.65 5
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14