Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11605020
LOC105369562
1.000 0.040 11 127110970 intron variant G/A;C snv 2
rs11608355
MYO1H
1.000 0.040 12 109441487 intron variant T/C snv 0.33 2
rs116362708
SLC44A5
1.000 0.040 1 75464629 intron variant G/A snv 2.3E-02 2
rs11663393
DCC
1.000 0.040 18 53088362 intron variant G/A snv 0.40 2
rs11664123
DCC
1.000 0.040 18 53440658 intron variant T/C snv 0.24 2
rs11693031
ERBB4
1.000 0.040 2 211813206 intron variant A/G;T snv 2
rs117198528
LOC105372112
1.000 0.040 18 49694188 intergenic variant T/G snv 1.0E-02 3
rs11826064 1.000 0.040 11 50818695 intergenic variant C/A;T snv 2
rs11924809
DGKG
0.925 0.040 3 186353656 intron variant G/A snv 5.3E-02 3
rs12030991 1.000 0.040 1 106683737 intergenic variant G/C;T snv 2
rs12068879
KAZN
1.000 0.040 1 14959860 intron variant A/G snv 0.18 2
rs12137398
CAMTA1
1.000 0.040 1 7730488 intron variant C/T snv 0.14 2
rs12137936
NEGR1
1.000 0.040 1 72254674 intron variant C/G snv 0.23 2
rs12420205 1.000 0.040 11 113523313 intergenic variant C/T snv 0.65 2
rs12457157
TCF4
1.000 0.040 18 55629696 intron variant G/A snv 0.41 2
rs1261070
TCF4
1.000 0.040 18 55235854 intron variant A/G snv 0.94 2
rs1261114
TCF4
1.000 0.040 18 55271138 intron variant G/A snv 0.46 2
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26 4
rs12938775
PAFAH1B1
1.000 0.040 17 2671527 intron variant G/A;T snv 2
rs12963463
TCF4
1.000 0.040 18 55431862 intron variant C/G;T snv 3
rs12967855
CELF4
1.000 0.040 18 37558282 intron variant A/G snv 0.52 2
rs13060816
BBX
1.000 0.040 3 107561639 intron variant T/A;C snv 2
rs13122395
EMCN
1.000 0.040 4 100829496 intron variant G/A snv 0.34 2
rs1322281
PTPRD
1.000 0.040 9 10582445 intron variant T/C snv 0.76 2
rs13296664 1.000 0.040 9 117684418 downstream gene variant C/T snv 0.22 2