Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1556425596
COL6A1
0.752 0.240 21 45989967 intron variant C/T snv 37
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 5
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 5
rs11585926
TRIM33
1.000 0.040 1 114431068 intron variant T/C snv 0.22 3
rs4327572 0.882 0.120 5 25972712 intron variant C/T snv 0.28 3
rs11102800
TRIM33
1.000 0.040 1 114498310 intron variant C/T snv 0.58 2
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 2
rs4765905
CACNA1C
0.827 0.040 12 2240418 intron variant G/A;C snv 2
rs4773054 1.000 0.040 13 109501681 intron variant T/C snv 0.89 2
rs7122539
PC
0.925 0.040 11 66895260 intron variant G/A snv 0.43 2
rs7741604
CDKAL1
0.925 0.120 6 20731293 intron variant A/C;T snv 2
rs9635542
PPL
1.000 0.040 16 4951379 intron variant A/G snv 0.11 2
rs10205350
GALNT14
1.000 0.040 2 30923631 intron variant G/T snv 0.24 1
rs10489525
CSDE1
1.000 0.040 1 114721064 intron variant G/A snv 0.32 1
rs10498676
ELOVL2
0.925 0.040 6 11026766 intron variant G/A snv 0.18 1
rs11118968
RASSF5
1.000 0.040 1 206524916 intron variant G/A snv 7.5E-02 1
rs11211996
GUCY1A2
1.000 0.040 11 106987949 intron variant T/C snv 0.15 1
rs11582563
TRIM33
1.000 0.040 1 114416918 intron variant G/A snv 0.14 1
rs11589568
TRIM33
1.000 0.040 1 114453702 intron variant T/C snv 0.14 1
rs12194182
SLC22A3
1.000 0.040 6 160413483 intron variant T/C snv 0.21 1
rs12331851
ZNF827
1.000 0.040 4 145928143 intron variant G/A snv 7.1E-02 1
rs12456492
RIT2
0.882 0.080 18 43093415 intron variant A/G snv 0.33 1