Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13404446
TRIM54
0.925 0.120 2 27296386 intron variant G/A snv 0.42 4
rs2305929
RBKS ; MRPL33 ; BABAM2-AS1 ; BABAM2
1.000 0.040 2 27891044 intron variant A/G snv 0.14 4
rs2877716
ADCY5
3 123375604 intron variant T/C snv 0.76 4
rs4665965
MPV17
0.925 0.120 2 27313513 intron variant T/A;C snv 4
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 4
rs780110
IFT172
0.925 0.120 2 27462521 intron variant G/A snv 0.56 4
rs853789
ABCB11
2 168944978 intron variant A/G;T snv 0.75 4
rs11717195
ADCY5
1.000 0.080 3 123363551 intron variant T/C snv 0.19 3
rs12055786
RGS17
6 153109990 intron variant C/T snv 0.46 3
rs1371614
DPYSL5
2 26930006 intron variant C/T snv 0.29 3
rs1401419
CRY2
1.000 0.040 11 45858188 intron variant T/C snv 0.39 3
rs1783598
FCHSD2
1.000 0.080 11 73140418 intron variant C/G;T snv 3
rs2908289
GCK ; LOC105375257
1.000 0.080 7 44184343 intron variant G/A snv 0.20 3
rs4245555
GRB10
1.000 0.120 7 50593712 intron variant T/C snv 0.32 3
rs4458523
WFS1
1.000 0.080 4 6288259 intron variant T/G snv 0.61 3
rs4869272
MIR583HG ; LOC101929710
5 96203744 intron variant C/T snv 0.72 3
rs7708285
ZBED3-AS1
1.000 0.080 5 77130042 intron variant G/A snv 0.76 3
rs7713317
LOC101929710
5 96381018 intron variant A/G snv 0.28 3
rs10278336
YKT6
7 44205764 intron variant A/C;G snv 2
rs10500292
SYMPK
19 45824675 intron variant C/T snv 0.46 2
rs11039119
MIR6745 ; PACSIN3
11 47180373 intron variant G/A snv 0.38 0.33 2
rs11039182
MADD
11 47325172 intron variant T/C snv 0.19 2
rs11607883 11 45818158 intron variant G/A snv 0.40 2
rs11619319
PLUT
13 27913462 intron variant A/G snv 0.23 2
rs11782386 8 9344277 intron variant C/T snv 9.7E-02 2