Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11603334
ARAP1
1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 3
rs11688682 1.000 0.080 2 120590036 intergenic variant G/C snv 0.20 3
rs1183910
HNF1A
1.000 0.080 12 120983004 intron variant G/A snv 0.28 3
rs12208357
SLC22A1
1.000 0.080 6 160122116 missense variant C/T snv 5.2E-02 4.9E-02 3
rs12692738
COBLL1
1.000 0.080 2 164701742 intron variant T/C snv 0.34 3
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 3
rs2000999
HPR ; TXNL4B
1.000 0.080 16 72074194 intron variant G/A snv 0.16 3
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 3
rs2250417
BCO2
1.000 0.080 11 112214593 intron variant T/C snv 0.44 3
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 3
rs35261542
CDKAL1
1.000 0.080 6 20675561 intron variant C/A snv 0.26 3
rs35658696
PAM
1.000 0.080 5 103003107 missense variant A/G snv 3.1E-02 3.2E-02 3
rs3764002
LOC105369965 ; WSCD2
1.000 0.080 12 108224853 missense variant C/T snv 0.27 0.20 3
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 3
rs4865796
ARL15
1.000 0.080 5 53976834 intron variant G/A snv 0.72 3
rs702634
ARL15
1.000 0.080 5 53975590 intron variant G/A snv 0.72 3
rs7034200
GLIS3
1.000 0.080 9 4289050 intron variant C/A;G snv 3
rs703978
ZMIZ1
1.000 0.080 10 79184390 intron variant C/G;T snv 0.68 3
rs7374732 1.000 0.080 3 23161963 regulatory region variant C/T snv 0.73 3
rs7578326
LOC646736
0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 3
rs7944584
MADD
1.000 0.080 11 47314769 intron variant A/T snv 0.19 3
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 3
rs9686661
C5orf67
1.000 0.080 5 56565959 intron variant C/T snv 0.20 3
rs9687833
C5orf67
1.000 0.080 5 56565774 intron variant G/A snv 0.21 3
rs10034465
LINC02484
1.000 0.080 4 34193882 intron variant G/A snv 9.1E-02 2