Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11119805
LPGAT1
1 211744902 3 prime UTR variant T/A snv 0.13 2
rs11120822
CAMTA1
1 7053052 intron variant G/C snv 0.34 2
rs2391388
ALG14
1 95020269 intron variant A/C snv 0.49 2
rs6671200
TLCD4-RWDD3 ; LOC101928118
1 95231973 intron variant A/C snv 0.90 2
rs6675668
ALG14
1 95050081 intron variant T/G snv 0.43 2
rs860873
CNN3
1 94921652 intron variant G/A snv 0.39 2
rs1514178
LOC101926964
1 60739797 intron variant T/C snv 1.5E-02 1
rs3845427 1 181293302 intergenic variant T/A snv 0.52 1
rs9437689 1 95083980 regulatory region variant C/T snv 0.34 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs2911711 0.925 0.120 2 27527679 downstream gene variant T/A snv 0.58 6
rs4666002
ZNF512
0.925 0.120 2 27617773 intron variant G/A;C snv 6
rs2118674
MYO3B
2 170462384 intron variant A/T snv 0.87 2
rs6722456 2 133771520 intergenic variant G/A snv 4.5E-02 2
rs12472274
ILKAP
2 238186781 non coding transcript exon variant G/A;T snv 1
rs1424760 2 162925277 intergenic variant C/T snv 0.52 1
rs16832011
LCT
2 135787729 downstream gene variant A/G snv 5.1E-02 1
rs334809
IL5RA
0.925 0.080 3 3088537 intron variant A/G;T snv 4
rs4453795
FGF12
3 192376186 intron variant A/G;T snv 2
rs197770
ITGA9
3 37474336 intron variant A/G snv 0.12 1
rs9832727
LOC100507389
3 142930268 intron variant C/A;G;T snv 1
rs10517480 4 59883111 intergenic variant A/T snv 0.27 2