Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1007863
SAMM50 ; PARVB
1.000 22 43999571 missense variant T/A;C snv 0.44 1
rs1010022
PNPLA3
1.000 22 43940430 intron variant A/G snv 0.20 1
rs1010023
PNPLA3
0.851 0.080 22 43940218 intron variant T/C snv 0.20 4
rs10499563
STEAP1B
0.807 0.120 7 22720869 intron variant T/C snv 0.21 7
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs11090617
PNPLA3
1.000 22 43930820 intron variant C/T snv 0.18 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12447924
CETP
1.000 16 56960280 upstream gene variant C/T snv 0.76 3
rs12483959
PNPLA3
1.000 22 43930116 intron variant G/A;C;T snv 4
rs12597002
CETP
1.000 16 56968492 intron variant C/A snv 0.25 3
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs12743824 0.925 0.040 1 99317401 intergenic variant C/A snv 0.48 2
rs1461729
LOC157273
1.000 8 9329732 intron variant A/G snv 0.88 5
rs1474745
PNPLA3
1.000 22 43953356 intron variant T/C snv 0.19 1
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 7
rs17107315
SPINK1
0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 40
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1883349
PNPLA3
1.000 22 43936063 intron variant G/A snv 0.19 1
rs1883350
PNPLA3
1.000 22 43932163 intron variant T/C snv 0.35 1
rs1977081
PNPLA3
1.000 22 43934248 intron variant T/C;G snv 2
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2071303
LOC108783645 ; HFE
0.882 0.120 6 26091108 splice region variant T/C snv 0.38 0.36 6