Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13122395
EMCN
1.000 0.040 4 100829496 intron variant G/A snv 0.34 2
rs11123857
NPAS2
2 100987350 non coding transcript exon variant A/G snv 0.29 1
rs188843168
ATP5MD
0.925 0.040 10 103390184 intron variant T/A;C snv 4.3E-04 3
rs11599236
SORCS3
1.000 0.040 10 104694914 intron variant T/C;G snv 2
rs1490176
SORCS3
1.000 0.040 10 104800467 intron variant T/A;G snv 2
rs1322281
PTPRD
1.000 0.040 9 10582445 intron variant T/C snv 0.76 2
rs7912226 1.000 0.040 10 105892386 intron variant T/A snv 0.44 2
rs12030991 1.000 0.040 1 106683737 intergenic variant G/C;T snv 2
rs2090408 1.000 0.040 3 107479604 intergenic variant G/T snv 0.32 2
rs836927 1.000 0.040 3 107482581 intergenic variant C/A snv 0.52 2
rs13060816
BBX
1.000 0.040 3 107561639 intron variant T/A;C snv 2
rs600011
BBX
1.000 0.040 3 107576545 intron variant A/C snv 0.25 2
rs11608355
MYO1H
1.000 0.040 12 109441487 intron variant T/C snv 0.33 2
rs2396133 1.000 0.040 7 109557010 intron variant A/G snv 0.47 2
rs4839421
CYMP
0.925 0.040 1 110479338 intron variant C/A snv 0.40 3
rs1940709
NCAM1
1.000 0.040 11 112978997 intron variant G/A snv 0.30 2
rs1940728
NCAM1
1.000 0.040 11 112981473 intron variant G/A;T snv 0.44 2
rs72995548
NCAM1 ; NCAM1-AS1
1.000 0.040 11 113268199 non coding transcript exon variant C/T snv 3.5E-02 2
rs2298489
TTC12
1.000 0.040 11 113364697 splice region variant A/G snv 0.61 2
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
rs10891564 1.000 0.040 11 113503291 intergenic variant G/A snv 0.34 2
rs35738585 1.000 0.040 11 113515625 intergenic variant T/G snv 0.40 2
rs12420205 1.000 0.040 11 113523313 intergenic variant C/T snv 0.65 2
rs7937477 1.000 0.040 11 113545374 intergenic variant A/T snv 0.59 2