Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11665867
SNRPA
19 40760574 intron variant A/G snv 0.13 1
rs4662402
TEX41
2 144886978 intron variant C/T snv 0.67 1
rs769651870
TFR2
7 100635310 intron variant T/A;C snv 1.2E-03 1
rs6745983
TMEM163
2 134673139 intron variant G/A snv 0.55 1
rs770551112
ZYG11A
1 52849688 intron variant -/CT;CTT ins 1
rs11039436 11 47866484 intergenic variant A/C;G;T snv 2
rs11730623 4 69020433 upstream gene variant A/T snv 0.66 2
rs11760376 7 134684558 intron variant A/G snv 1.9E-03 2
rs1340817 13 28656444 upstream gene variant A/G snv 0.47 2
rs149823406 7 100716851 upstream gene variant C/T snv 4.6E-03 2
rs6126019 20 50485053 intergenic variant T/C snv 0.58 2
rs61642945 X 8911833 intron variant C/T snv 2
rs6967414 7 6710127 upstream gene variant G/A snv 0.29 2
rs78003500 6 43763914 regulatory region variant G/A;T snv 2
rs9614727 22 45629162 upstream gene variant G/A snv 0.11 2
rs9697691 22 45914013 intergenic variant C/G snv 0.43 2
rs972761 5 34507680 intergenic variant T/C snv 0.40 2
rs342437
AFF1
4 87119757 intron variant A/G snv 0.65 2
rs7312105
CACNA1C
12 2414189 intron variant A/G snv 0.34 2
rs662735
DCDC1 ; LOC105376611
11 30881895 intron variant T/A;G snv 2
rs2742540
DENND2B
11 8877981 intron variant A/G snv 0.41 2
rs806293
DLEU1
13 50238846 intron variant T/A snv 0.47 2
rs34121753
DNAH2
17 7830515 intron variant A/G snv 0.40 0.41 2
rs797343
EGLN3 ; LOC102724945
14 34177063 intron variant C/T snv 0.73 2
rs62482253
GNB2
7 100677821 splice region variant G/A snv 2.6E-03 2.8E-03 2