Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17789218
LOC105377911
6 100152221 intergenic variant T/A;C snv 3
rs17883880
CHUK
10 100230590 intron variant T/A snv 1.2E-02 4
rs7904983
PKD2L1
10 100296259 stop gained G/A;C snv 1.4E-02; 4.1E-06 1
rs7909153
PKD2L1
10 100297033 missense variant G/A snv 1.3E-02 5.2E-02 1
rs8071787
GAS7
17 10058819 intron variant T/C snv 4.8E-02 5
rs3783599
VCAM1
1 100718331 upstream gene variant C/T snv 1.6E-02 1
rs3917056
VCAM1
1 100730346 intron variant G/C snv 2.5E-02 1
rs35404864
NOX1
X 100850151 missense variant C/T snv 7.0E-03 2.5E-02 1
rs6542999
NPAS2
2 100937295 intron variant T/C;G snv 1
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs2227700
SERPINE1
7 101138800 3 prime UTR variant T/C snv 1.2E-02 1
rs11247287
PCSK6
15 101365328 intron variant T/C snv 0.34 1
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs1398607 1.000 0.080 3 102036894 TF binding site variant C/A;T snv 2
rs17779355 10 102168617 downstream gene variant G/A snv 4.1E-02 1
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs5742683
LINC02456 ; IGF1
12 102419939 intron variant A/G snv 3.3E-02 1
rs5742663
IGF1 ; LINC02456
12 102430212 intron variant T/A;G snv 1
rs7300373
IGF1 ; LINC02456
12 102438008 intron variant T/G snv 1.4E-02 1
rs13401597
IL18RAP
2 102444358 intron variant C/G snv 1.8E-02 1
rs5742626
LINC02456 ; IGF1
12 102464131 intron variant T/C snv 2.3E-02 3
rs5742617
IGF1
12 102476127 intron variant C/T snv 8.7E-03 1
rs2075847
WTAPP1 ; MMP1
11 102799093 intron variant A/C;G snv 3
rs5030383
ICAM1 ; ICAM4
19 10286167 3 prime UTR variant C/A;T snv 1