Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 10
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 7
rs2710323
ITIH1
0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs12576775
TENM4
0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 6
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 5
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 5
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 5
rs10994397
ANK3
0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 5
rs11152369
TCF4
0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs12325410
LOC101927026
0.851 0.040 16 9581389 intron variant T/G snv 0.16 5
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 5
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 5
rs190065944
CHRNA5
0.925 0.080 15 78567268 intron variant G/A snv 3.4E-03 5
rs2021722
TRIM26
0.851 0.040 6 30206354 intron variant C/A;T snv 0.24 5
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 5
rs2721800
MPP6
0.851 0.040 7 24652933 intron variant G/A;C;T snv 5