Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1015538
ZKSCAN1
7 100028412 intron variant A/G snv 0.72 1
rs66803065
SBF2
11 10004305 intron variant C/A;T snv 0.19 2
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs71476638 11 100648287 intergenic variant G/A;T snv 4.0E-02 1
rs2978098
LOC105375672 ; SNX31
8 100664447 upstream gene variant A/C;T snv 1
rs6590811
ARHGAP42
11 100708153 intron variant C/T snv 0.53 4
rs1502284
ARHGAP42
11 100713419 intron variant T/A;G snv 2
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs6590816
ARHGAP42
11 100730902 intron variant G/A snv 0.40 4
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs486023
ARHGAP42
11 100772406 intron variant G/A snv 0.25 2
rs4551692
PAX2
10 100796696 intron variant G/A snv 0.91 2
rs138475089 7 100899019 upstream gene variant -/TA delins 1
rs2062331
MSRA
8 10122482 intron variant A/G snv 0.51 2
rs61892344 11 101230037 intergenic variant C/G;T snv 1
rs72847884
BTRC
10 101355588 intron variant A/G snv 2.4E-02 1
rs56290975
SENP7
3 101509521 intron variant G/A;C snv 1
rs17248480
BANK1
4 101514108 intron variant G/A snv 1.8E-02 2
rs11923667 3 101549236 regulatory region variant T/A snv 0.40 1
rs150834401 4 102243067 intergenic variant C/T snv 3.2E-02 1
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs34919878
MSRA
8 10241994 intron variant G/A snv 0.29 2
rs284844
WBP1L
10 102794772 intron variant A/G snv 0.82 3
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13