Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4919624
GBF1
10 102261328 intron variant A/G snv 0.16 1
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1016162 3 102299 regulatory region variant C/T snv 0.36 1
rs72845663
GBF1
10 102321592 intron variant C/T snv 0.32 1
rs10088255
UBR5
8 102355371 intron variant A/T snv 0.55 1
rs4734619
UBR5
8 102377272 intron variant C/G snv 0.77 1
rs12434396
TRAF3
14 102816265 intron variant C/G;T snv 1
rs80134320
PAM
5 102834090 intron variant G/T snv 3.1E-02 1
rs17151637
MSRA
8 10295572 intron variant C/G;T snv 2
rs10202535
TMEM182
2 102957679 intron variant T/C snv 0.61 1
rs4380261
TMEM182
2 102962092 intron variant G/T snv 0.61 1
rs79001489
MSRA
8 10303578 intron variant C/A snv 0.10 1
rs17028556 2 103284125 intergenic variant G/T snv 0.22 1
rs187580 5 103291654 intergenic variant T/G snv 0.16 1
rs2642365
LOC105369147 ; BAALC-AS1
8 103296005 intron variant C/A;T snv 1
rs7832708
MSRA
8 10332530 intron variant C/T snv 0.49 4
rs76160968 5 103346444 TF binding site variant A/G;T snv 3.0E-02 2
rs10233848
LOC101927870 ; RELN
7 103482198 non coding transcript exon variant A/G snv 0.42 1
rs71415374 2 103538956 intergenic variant C/T snv 5.7E-02 1
rs10129426 14 103552118 upstream gene variant G/A snv 0.54 2
rs729437
KLC1 ; LOC105370688
14 103627184 intron variant C/G;T snv 2
rs6776198 3 103649166 intergenic variant G/A snv 0.28 1
rs57714592 3 103720486 intergenic variant T/C snv 0.30 1
rs2570495 2 103827484 intergenic variant C/T snv 0.54 1
rs1550536 2 103834676 intergenic variant C/G snv 0.55 1