Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4849133 2 112923864 downstream gene variant C/A;T snv 2
rs1281032650
LNPEP
5 96979168 missense variant A/G snv 1
rs1290547844
BRD4
19 15273041 missense variant C/T snv 4.0E-06 1
rs1316569885
SORBS1
10 95399139 missense variant C/T snv 4.0E-06 7.0E-06 1
rs1325863623
SERPINB6
6 2953175 missense variant C/T snv 4.0E-06 1
rs1921
ISG15
1 1014228 missense variant G/A;C snv 0.36 1
rs200192581
SORBS1
10 95381729 missense variant C/T snv 8.0E-06 7.0E-06 1
rs2071025
COL11A2
6 33175979 intron variant A/G snv 0.28 0.29 1
rs3116996 6 33130187 downstream gene variant T/A snv 0.13 1
rs7314777
LOC105369818
12 68256855 upstream gene variant T/C snv 0.19 1
rs751703423
AIMP2 ; EIF2AK1
7 6023410 missense variant G/A;C snv 1
rs778438430
SORBS1
10 95381747 missense variant C/T snv 1.6E-05 2.8E-05 1
rs779770523
SORBS1
10 95432543 missense variant C/G;T snv 1.2E-05; 4.0E-06 1
rs781314841
SORBS1
10 95341566 missense variant C/T snv 4.4E-05 2.8E-05 1
rs868564661
FGFR2
10 121487415 missense variant G/A snv 1
rs954917585
FGFR2
10 121479973 missense variant G/A snv 8.0E-06 1.4E-05 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116