Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 3
rs1783598
FCHSD2
1.000 0.080 11 73140418 intron variant C/G;T snv 3
rs2305929
RBKS ; MRPL33 ; BABAM2-AS1 ; BABAM2
1.000 0.040 2 27891044 intron variant A/G snv 0.14 3
rs2877716
ADCY5
3 123375604 intron variant T/C snv 0.76 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
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 3
rs7651090
IGF2BP2
0.925 0.080 3 185795604 intron variant A/G snv 0.39 3
rs7708285
ZBED3-AS1
1.000 0.080 5 77130042 intron variant G/A snv 0.76 3
rs7944584
MADD
1.000 0.080 11 47314769 intron variant A/T snv 0.19 3
rs853789
ABCB11
2 168944978 intron variant A/G;T snv 0.75 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
rs11672660
GIPR ; MIR642B
19 45676926 intron variant C/T snv 0.18 0.17 2
rs11782386 8 9344277 intron variant C/T snv 9.7E-02 2
rs11891554
PPM1G
2 27390750 intron variant G/A;T snv 7.1E-02 2
rs12055786
RGS17
6 153109990 intron variant C/T snv 0.46 2
rs1280 3 170995501 intron variant T/C snv 0.20 2
rs1401419
CRY2
1.000 0.040 11 45858188 intron variant T/C snv 0.39 2
rs16913693
ELP1
9 108918079 intron variant T/G snv 8.4E-02 2