Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 5
rs10489744
RXRG
0.925 0.040 1 165411386 intron variant G/A snv 0.55 2
rs10492664 0.925 0.040 13 108163877 intergenic variant C/A;T snv 2
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs10514604
ATP2C2
1.000 0.040 16 84412778 intron variant C/A;G snv 1
rs10826548 1.000 0.040 10 28966665 intergenic variant C/A snv 0.13 1
rs10910623
MAP10
1.000 0.040 1 232802953 upstream gene variant G/A snv 7.5E-02 1
rs10956838 1.000 0.040 8 92392214 intergenic variant A/C snv 0.28 2
rs10983238
LOC107987015 ; ASTN2
1.000 0.040 9 116571404 intron variant C/A;G snv 0.16 1
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
rs11074889
EMP2
1.000 0.040 16 10539308 intron variant A/G;T snv 1
rs11152369
TCF4
0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs11162556 0.925 0.040 1 78795698 intergenic variant A/G snv 0.32 2
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 10
rs11210887
PTPRF
0.925 0.040 1 43610348 intron variant G/A snv 0.52 2
rs11243897
AK8
1.000 0.040 9 132742896 intron variant A/G snv 0.33 1
rs112984125
ST3GAL3 ; KDM4A-AS1
1.000 0.040 1 43707752 intron variant G/A snv 0.25 1
rs11317767
LOC105371529
1.000 0.040 17 8770824 intergenic variant TTT/-;TT;TTTT delins 1
rs113551349
SLC6A9
0.925 0.040 1 44009451 intron variant C/T snv 0.20 2
rs114181198 1.000 0.040 2 183618431 intergenic variant C/A snv 1
rs114247285
SV2C
1.000 0.040 5 76044157 intergenic variant G/A snv 3.8E-02 1
rs11514810 1.000 0.040 7 1388840 intergenic variant C/T snv 0.19 1
rs11591402
SORCS3
1.000 0.040 10 104987596 intron variant T/A;G snv 1