Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4821480
MYH9
0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs756322971
CASR
0.763 0.240 3 122284955 missense variant C/A;G snv 9
rs16840252
CTLA4
0.776 0.480 2 203866796 upstream gene variant C/T snv 0.16 8
rs17173608
RARRES2
0.807 0.240 7 150339575 intron variant T/G snv 0.11 8
rs3448
GPX1 ; RHOA
0.776 0.240 3 49359318 3 prime UTR variant T/C snv 0.76 8
rs3957357
GSTA1
0.807 0.280 6 52803889 upstream gene variant A/G snv 0.63 7
rs452204
IL1RN
0.807 0.200 2 113131484 intron variant G/A snv 0.45 7
rs12513649 0.851 0.160 5 173045049 regulatory region variant C/G;T snv 6
rs10951982
RAC1
0.851 0.160 7 6382925 intron variant G/A;T snv 5
rs11089788
MYH9
0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs1452199941
TBC1D9
0.827 0.160 4 140670787 missense variant T/C snv 7.0E-06 5
rs777476179
ALMS1
0.851 0.280 2 73448259 frameshift variant A/- del 1.4E-05 5
rs13447075
PVT1
0.882 0.120 8 127998344 non coding transcript exon variant C/A snv 4
rs2648862
PVT1 ; MIR1207
0.882 0.120 8 128049539 non coding transcript exon variant C/A snv 2.9E-02 4
rs379489
CFH
0.851 0.200 1 196724321 intron variant A/G snv 0.65 4
rs4730751
CAV1
0.882 0.120 7 116540796 intron variant C/A snv 0.22 4
rs730497
GCK ; LOC105375257
0.882 0.160 7 44184122 intron variant G/A snv 0.17 4
rs743811 0.882 0.160 22 35396981 upstream gene variant T/A;C snv 4
rs75444904
HPR ; TXNL4B
0.851 0.160 16 72061751 intron variant A/C snv 2.4E-02 4
rs7588550
ERBB4
0.851 0.160 2 212304043 intron variant G/A snv 0.96 4
rs867394500
ACE
0.851 0.080 17 63477301 missense variant G/T snv 4
rs1033182
ESR1
0.882 0.160 6 151873899 intron variant G/A snv 0.26 3
rs1057518923
PKD1
0.925 0.200 16 2115395 frameshift variant -/C delins 3
rs11571317
CTLA4
0.882 0.160 2 203867285 upstream gene variant C/T snv 5.2E-02 3
rs1162592300
ALB
0.925 0.080 4 73412045 missense variant G/A snv 3