Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs3176867
VCAM1
1 100728649 intron variant C/A;T snv 1
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs10748798
PAX2
10 100794914 intron variant C/T snv 0.91 1
rs763802417
NOX1
0.882 0.040 X 100862805 missense variant G/A snv 5.9E-06 5
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs9806366 15 101262752 intergenic variant C/T snv 0.24 1
rs28628459
SELENOS
15 101272152 intron variant T/C snv 0.25 1
rs12917258
SELENOS
15 101273134 intron variant C/G snv 0.19 1
rs4965814
SELENOS
1.000 0.080 15 101273712 intron variant C/T snv 0.62 2
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs1074703
NCALD
8 101803258 intron variant C/A snv 0.63 1
rs13127398
BANK1
4 102000547 intron variant T/A snv 4.1E-02 1
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs5491
ICAM1
0.827 0.160 19 10274864 missense variant A/G;T snv 4.0E-06; 2.8E-02 6
rs281432
ICAM1
0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs10903323
MSRA
0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs7681002
SLC9B1
4 102974066 intron variant A/G snv 0.57 1
rs2513993
DCUN1D5
11 103082247 intron variant A/G snv 0.32 1