Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10849433
LOC105369624
0.776 0.080 12 6297738 regulatory region variant T/C snv 0.38 10
rs10980628
LPAR1
0.776 0.080 9 110909123 intron variant T/C snv 0.16 10
rs11085466
LOC101929007
0.790 0.080 19 21569009 intron variant G/C snv 0.23 10
rs11087784 0.776 0.080 20 7760329 intergenic variant A/G snv 0.13 10
rs11150038
CLEC3A
0.790 0.080 16 78042662 intron variant A/C;G snv 10
rs11169552
ATF1
0.776 0.080 12 50761880 upstream gene variant C/T snv 0.23 10
rs11190164 0.776 0.080 10 99591947 intergenic variant A/G snv 0.19 10
rs11196170
TCF7L2
0.776 0.080 10 112962862 intron variant G/A;C snv 10
rs11610543 0.776 0.080 12 42740389 intergenic variant A/G;T snv 10
rs116353863 0.776 0.080 6 31042408 regulatory region variant T/C snv 2.2E-02 10
rs11692435
ACTR1B
0.790 0.080 2 97658891 missense variant G/A snv 7.0E-02 6.7E-02 10
rs117079142
LOC112268030 ; UTP23
0.776 0.080 8 116778675 intron variant C/A snv 3.0E-02 10
rs11884596
LOC105373831
0.776 0.080 2 198747683 intron variant T/C snv 0.32 10
rs12144319
TTC22
0.776 0.080 1 54780362 3 prime UTR variant T/C snv 0.31 10
rs12149163 0.776 0.080 16 86305709 upstream gene variant T/C snv 0.49 10
rs12246635
VTI1A
0.776 0.080 10 112528860 intron variant T/C snv 0.13 10
rs12372718
ATF1
0.776 0.080 12 50777307 intron variant A/G snv 0.35 10
rs12447408 0.776 0.080 16 86218938 downstream gene variant G/A snv 0.21 10
rs1250567
ZMIZ1
0.776 0.080 10 79286508 intron variant T/C snv 0.56 10
rs12514517 0.776 0.080 5 40279974 intergenic variant G/A snv 0.21 10
rs12594720
SMAD6
0.776 0.080 15 66714680 intron variant C/G snv 0.23 10
rs12646351
ZNF827
0.790 0.080 4 145819473 intron variant G/A snv 0.19 10
rs12672022 0.776 0.080 7 45096824 downstream gene variant T/C snv 0.13 10
rs12708491 0.776 0.080 15 32700635 downstream gene variant G/A snv 0.33 10
rs13086367 0.776 0.080 3 113185041 downstream gene variant A/G snv 0.38 10