Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9393903
ELOVL2 ; ELOVL2-AS1
6 11042676 intron variant G/A snv 0.18 3
rs494562 6 85407411 intergenic variant A/G snv 0.16 2
rs662138
SLC22A1
6 160143444 intron variant C/G snv 0.14 2
rs9358356
CDKAL1
1.000 0.080 6 20667151 intron variant T/C snv 0.39 1
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 4
rs10244051 1.000 0.080 7 15024208 intergenic variant T/A;G snv 3
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 3
rs17277546
TRIM4
7 99891948 3 prime UTR variant G/A snv 3.1E-02 3
rs12670403
LOC101927609 ; AHR
7 17269655 intron variant C/A snv 0.46 2
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 2
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 2
rs1558318 1.000 0.080 7 15025987 intergenic variant A/T snv 0.55 1
rs2971672
GCK
7 44166307 intron variant A/C snv 0.44 1
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 3
rs1495743 8 18415790 intergenic variant G/A;C snv 2
rs6558295
GPAA1
8 144084619 intron variant C/G snv 8.1E-02 0.14 2
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 4
rs7094971
SLC16A9
0.925 0.120 10 59689806 intron variant A/G snv 0.13 4
rs11185790
PANK1
10 89612776 intron variant G/A snv 0.15 2