Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs6725887
WDR12
0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02 4
rs1561198
VAMP5
0.882 0.120 2 85582866 upstream gene variant C/T snv 0.52 3
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs12190287
TCF21
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19
rs2281727
SMG6
0.882 0.080 17 2214651 intron variant A/G snv 0.38 4
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs17114036
PLPP3
0.851 0.120 1 56497149 intron variant A/G snv 0.11 5
rs9369640
PHACTR1
0.851 0.080 6 12901209 intron variant C/A;G snv 4
rs9818870
MRAS
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 9
rs7173743
MORF4L1
0.851 0.120 15 78849442 intron variant T/C snv 0.45 6
rs121918529
MEF2A
0.882 0.080 15 99690400 missense variant C/T snv 6.1E-04 6.5E-04 3
rs121918531
MEF2A
0.925 0.080 15 99690412 missense variant G/A snv 8.3E-06 2.1E-05 2
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 16
rs2246833
LIPA
0.882 0.080 10 89246097 intron variant C/T snv 0.38 3
rs11203042
LIPA
1.000 0.080 10 89229352 intron variant T/A;C snv 1
rs10947789
KCNK5
0.925 0.080 6 39207146 intron variant T/C snv 0.18 2
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs2895811
HHIPL1
0.851 0.080 14 99667605 intron variant T/A;C snv 4
rs2642
GOT1
1.000 0.080 10 99396992 3 prime UTR variant T/C snv 5.0E-02 1
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 7
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs3217992
CDKN2B-AS1 ; CDKN2B
0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22