Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10020288 1.000 0.040 4 28686220 intergenic variant G/A snv 0.38 2
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs10144845
YLPM1
1.000 0.040 14 74771067 intron variant C/T snv 0.62 2
rs10156548 1.000 0.040 9 23318435 intron variant G/C;T snv 2
rs10405382
DPY19L3 ; LOC400684
1.000 0.040 19 32405810 5 prime UTR variant C/G snv 0.18 2
rs10429537 1.000 0.040 9 23346844 intron variant C/G snv 0.33 2
rs1055447
ARFGAP2 ; C11orf49
1.000 0.040 11 47164873 3 prime UTR variant C/A;T snv 2
rs10891564 1.000 0.040 11 113503291 intergenic variant G/A snv 0.34 2
rs10950393
TMEM106B
1.000 0.040 7 12223920 intron variant T/C snv 0.50 2
rs10965780 1.000 0.040 9 23341717 intron variant C/G;T snv 3
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 2
rs11039149
NR1H3
0.827 0.280 11 47255124 intron variant A/G snv 0.19 2
rs11039409
NUP160
1.000 0.040 11 47814169 intron variant A/C snv 0.22 2
rs11123857
NPAS2
2 100987350 non coding transcript exon variant A/G snv 0.29 1
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs11152363
TCF4
1.000 0.040 18 55389957 intron variant G/A snv 0.16 2
rs11209175
GNG12-AS1
1.000 0.040 1 67909145 intron variant C/T snv 0.54 2
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs11214589
TTC12
1.000 0.040 11 113374326 intron variant G/A snv 0.36 2
rs11214607
DRD2
1.000 0.040 11 113441417 intron variant T/G snv 0.16 2
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs113378111 1.000 0.040 2 9788024 intergenic variant G/A snv 2.8E-02 3
rs114465512
IGLV10-54
1.000 0.040 22 22047895 intron variant C/T snv 4.7E-03 3
rs11514731
MAD1L1
1.000 0.040 7 2011868 intron variant C/G snv 0.16 2
rs11599236
SORCS3
1.000 0.040 10 104694914 intron variant T/C;G snv 2