Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 6
rs16991720
KCNE1
21 34484464 intron variant A/C snv 4
rs480392
NTNG1
1 107436774 synonymous variant A/C snv 0.99 0.95 3
rs6726798
VIL1
2 218436132 intron variant A/C snv 0.94 3
rs7000460
LPL
8 19946291 intron variant A/C snv 7.9E-02 3
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 2
rs34515106
PLEK
2 68380846 missense variant A/C snv 6.7E-03 1.9E-03 2
rs12158587
GRK3
22 25623573 intron variant A/C snv 2.8E-02 1
rs1351452
SIK3
11 117072638 intron variant A/C snv 0.86 1
rs2227368
CPAMD8
19 16896136 non coding transcript exon variant A/C snv 6.6E-03 2.6E-02 1
rs2971672
GCK
7 44166307 intron variant A/C snv 0.44 1
rs3827216
APP
21 25924954 intron variant A/C snv 1.7E-02 1
rs453789
LOC105371789 ; HDAC5
17 44118647 intron variant A/C snv 0.97 1
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 1
rs6872314
CERT1
5 75440240 intron variant A/C snv 0.35 1
rs6951033 7 142636699 upstream gene variant A/C snv 0.12 1
rs7926960
ZPR1
11 116783370 intron variant A/C snv 1.5E-02 1
rs8077889
MPP3
17 43800798 downstream gene variant A/C snv 0.19 1
rs9340922
ESR1
6 151971471 intron variant A/C snv 5.1E-02 1
rs9972882
STARD3
0.925 0.080 17 39651445 intron variant A/C snv 0.66 1
rs2075847
WTAPP1 ; MMP1
11 102799093 intron variant A/C;G snv 3
rs11207995
DOCK7
1 62583880 intron variant A/C;G snv 2
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 2
rs1975802
PLA2G15
1.000 0.040 16 68251944 intron variant A/C;G snv 2
rs16981094
TPM4
19 16078757 intron variant A/C;G snv 3.3E-02 1