Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 1
rs10084572
LOC105372829
1.000 0.040 21 43992991 downstream gene variant T/A;C;G snv 3
rs10116772
GLIS3
0.882 0.080 9 4290541 intron variant C/A;T snv 2
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 8
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 8
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs10486567
JAZF1
0.851 0.120 7 27936944 intron variant G/A snv 0.28 2
rs10494366
LOC105371475 ; NOS1AP
0.851 0.200 1 162115895 intron variant G/T snv 0.54 1
rs10497721
LOC101927366 ; TMEFF2
1.000 0.040 2 192049636 intron variant C/A;T snv 2
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 6
rs10517086
LINC02357
0.882 0.160 4 26083889 intron variant G/A snv 0.27 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 2
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs10757272
CDKN2B-AS1
0.851 0.160 9 22088261 intron variant C/T snv 0.41 2
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
rs10811652
CDKN2B-AS1
0.882 0.120 9 22077086 intron variant A/C;T snv 3
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 3
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 7
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 2
rs10941191 1.000 0.040 5 34504693 intergenic variant C/A;T snv 3
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 1
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 3