Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10150332
NRXN3
14 79470621 intron variant T/C snv 0.26 4
rs10769908
STK33
11 8462542 intron variant C/T snv 0.55 4
rs11161721
COL24A1
1 86022231 intron variant C/A snv 0.27 0.27 4
rs11663816 18 60208994 intergenic variant T/C snv 0.20 4
rs12328675
COBLL1
2 164684290 3 prime UTR variant T/C snv 0.13 4
rs12429545 13 53528071 intron variant G/A;T snv 0.12 4
rs12714415 2 651430 intergenic variant T/C snv 0.19 4
rs12885454
LOC102724934
14 29267632 non coding transcript exon variant C/A snv 0.27 4
rs17024393
GNAT2
1 109612066 intron variant T/C snv 4.6E-02 4
rs177430
NPC1 ; RMC1
18 23506161 intron variant C/A;T snv 4
rs1982350
ARNTL
11 13328584 intron variant A/G snv 0.57 4
rs2033529
TDRG1
6 40380914 intron variant A/C;G snv 4
rs2145270 20 6641038 regulatory region variant C/T snv 0.61 4
rs2877716
ADCY5
3 123375604 intron variant T/C snv 0.76 4
rs306890
SPRY3
Y 56944005 intergenic variant T/C snv 4
rs34720381
PRRC2C
1 171486183 intron variant C/T snv 7.3E-02 4
rs4691380
PDGFC
4 156798972 intron variant C/T snv 0.45 4
rs4715210 6 50929538 regulatory region variant C/G;T snv 4
rs4776970
MAP2K5
15 67788548 intron variant A/T snv 0.44 4
rs4985155
PDXDC1
16 15035602 intron variant A/G snv 0.40 0.37 4
rs60808706
KCNQ1
11 2836003 intron variant G/A snv 0.12 4
rs61754230
RAB21
12 71785666 missense variant C/T snv 1.3E-02 1.2E-02 4
rs62104180 2 466003 intergenic variant G/A snv 2.9E-02 4
rs6545714 2 59080590 intron variant G/A;C snv 4
rs6809651
ETV5
3 186096853 intron variant G/A snv 0.14 4