Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2642
GOT1
1.000 0.080 10 99396992 3 prime UTR variant T/C snv 5.0E-02 1
rs11203042
LIPA
1.000 0.080 10 89229352 intron variant T/A;C snv 1
rs2246833
LIPA
0.882 0.080 10 89246097 intron variant C/T snv 0.38 1
rs2047009 0.925 0.080 10 44044465 regulatory region variant T/G snv 0.39 2
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 2
rs10947789
KCNK5
0.925 0.080 6 39207146 intron variant T/C snv 0.18 2
rs9369640
PHACTR1
0.851 0.080 6 12901209 intron variant C/A;G snv 2
rs2281727
SMG6
0.882 0.080 17 2214651 intron variant A/G snv 0.38 2
rs1561198
VAMP5
0.882 0.120 2 85582866 upstream gene variant C/T snv 0.52 2
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 3
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 3
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 3
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 3
rs2895811
HHIPL1
0.851 0.080 14 99667605 intron variant T/A;C snv 3
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 3
rs7173743
MORF4L1
0.851 0.120 15 78849442 intron variant T/C snv 0.45 3
rs9818870
MRAS
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 3
rs17114036
PLPP3
0.851 0.120 1 56497149 intron variant A/G snv 0.11 3
rs12190287
TCF21
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 3
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 3
rs9982601 0.851 0.080 21 34226827 intron variant C/T snv 0.15 4
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 4
rs6725887
WDR12
0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02 4
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 6
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6