Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201721079
LEPR
1 65615104 intron variant -/C delins 1
rs35308591
LEPR
1 65615104 intron variant -/C delins 1
rs36066893
CR1
1 207620619 intron variant -/T delins 1
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 7
rs10518765
UNC13C
1.000 0.040 15 54388434 intron variant A/C snv 0.16 3
rs17519972
GLMN ; RPAP2
1.000 0.080 1 92362948 intron variant A/C snv 0.15 2
rs3845624 1 159248476 regulatory region variant A/C snv 0.57 2
rs75460349
ZDHHC18
1 26853597 intron variant A/C snv 1.7E-02 2
rs13386602 2 113077243 downstream gene variant A/C snv 0.56 1
rs1867939 1 159636104 intergenic variant A/C snv 0.32 1
rs2608928 6 131470731 upstream gene variant A/C snv 0.75 1
rs2647062
HLA-DRB1
6 32602640 intergenic variant A/C snv 0.13 1
rs3026943 1 159162136 intergenic variant A/C snv 0.57 1
rs6513566 20 61225053 intergenic variant A/C snv 0.60 1
rs4660293
PABPC4
1 39562508 non coding transcript exon variant A/C;G snv 5
rs7979473
HNF1A
12 120982457 intron variant A/C;G snv 2
rs1169303
HNF1A
12 120998573 intron variant A/C;G snv 0.45 1
rs1441169
LINC01953 ; LOC105373864
2 213168806 upstream gene variant A/C;G snv 1
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 9
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 7
rs12034864 1 159215190 regulatory region variant A/C;G;T snv 2
rs7979478
HNF1A
12 120982460 intron variant A/C;G;T snv 2
rs4083420 1 159225048 intergenic variant A/C;G;T snv 1
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57