Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 4
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs10150332
NRXN3
14 79470621 intron variant T/C snv 0.26 3
rs10769908
STK33
11 8462542 intron variant C/T snv 0.55 3
rs12967135 18 60181790 intergenic variant G/A snv 0.24 3
rs1371614
DPYSL5
2 26930006 intron variant C/T snv 0.29 3
rs2877716
ADCY5
3 123375604 intron variant T/C snv 0.76 3
rs10136789
KCNH5
14 62889535 intron variant T/C snv 0.15 2
rs10261878 7 25910925 intergenic variant A/C snv 0.80 2
rs10789336
LOC105378797
1 72372723 intron variant G/A;C snv 2
rs10993160 9 94306644 downstream gene variant A/G snv 4.2E-02 2
rs1106683 7 131768766 intergenic variant G/A snv 0.14 2
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 2
rs11672660
GIPR ; MIR642B
19 45676926 intron variant C/T snv 0.18 0.17 2
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 2
rs11951673
LOC101929710 ; CAST
5 96525308 non coding transcript exon variant C/T snv 0.39 2
rs12328675
COBLL1
2 164684290 3 prime UTR variant T/C snv 0.13 2
rs12597579 16 20246545 intergenic variant C/A;T snv 2
rs12714415 2 651430 intergenic variant T/C snv 0.19 2
rs12964056 18 60006567 upstream gene variant A/G;T snv 2
rs1542829
COL6A5
3 130418627 intron variant G/A snv 8.0E-02 2
rs1555543 1 96479241 intergenic variant A/C snv 0.55 2
rs1561288
EFR3B
2 25146133 3 prime UTR variant C/T snv 0.29 2
rs16858082 4 45173787 intergenic variant T/C snv 0.41 2
rs17124318
LINC01739
1 63015059 intron variant C/A;G;T snv 2