Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12135191 1 236307434 regulatory region variant C/G;T snv 2
rs12313306
R3HDM2
12 57358071 intron variant C/T snv 0.19 2
rs12693043 2 174512837 intergenic variant C/T snv 0.36 2
rs12987661
AAK1
2 69586326 intron variant T/C snv 0.11 2
rs13069049 3 66759518 intergenic variant A/T snv 0.15 2
rs13116011 4 136424394 intergenic variant T/A;C snv 2
rs147287428
LRP2
2 169206713 missense variant C/T snv 2.7E-04 4.7E-04 2
rs16886173 8 114608231 intergenic variant T/G snv 7.5E-02 2
rs17079585
ANKRD20A19P
13 23921903 regulatory region variant G/A snv 1.9E-02 2
rs1797052
PDZK1
1 145707383 5 prime UTR variant A/G;T snv 2
rs1917861 11 80678655 intergenic variant A/G;T snv 2
rs2077393
CARMIL1
6 25607137 intron variant C/T snv 0.29 2
rs2834319
LOC105372790
21 33984724 regulatory region variant T/C snv 0.16 2
rs28362590
RAB24 ; PRELID1 ; MXD3
5 177304451 intron variant G/C;T snv 0.78 2
rs2950835 2 27527678 downstream gene variant A/G;T snv 2
rs35198068
TCF7L2
10 112995025 intron variant T/C snv 0.29 2
rs3741210
INS-IGF2 ; IGF2 ; IGF2-AS
11 2148310 non coding transcript exon variant A/G snv 0.30 2
rs3904600
RREB1
6 7109432 intron variant C/G snv 0.46 2
rs429479
OR5V1 ; OR12D3
6 29404546 intron variant A/G;T snv 2
rs4767631
KSR2
12 117873938 intron variant G/A;C snv 2
rs62052820 16 69541335 intergenic variant G/A snv 0.17 2
rs6569474
RSPO3 ; LOC112267972
6 127172466 intron variant A/T snv 0.54 2
rs6911965
GPLD1
6 24480067 intron variant T/A;C snv 2
rs7209801 17 44246008 downstream gene variant G/A snv 0.38 2
rs7212936
SERPINF2
17 1743357 intron variant A/C snv 0.46 2