Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 5
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 5
rs2249105
CEP68
2 65060762 intron variant A/G snv 0.40 5
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 5
rs2763981
CYP21A2 ; SLC44A4
6 31872244 intron variant T/A snv 0.79 5
rs2845885
FLRT1 ; MACROD1
11 64101590 intron variant C/T snv 0.87 5
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 5
rs661171
ZC3H12C ; RDX
11 110145794 intron variant T/G snv 0.69 5
rs7096937
GPAM
10 112190660 intron variant T/C snv 0.72 5
rs74617384
LPA
0.925 0.080 6 160576086 intron variant A/G;T snv 5
rs7890572
IL1RAPL1
X 29622701 intron variant A/G snv 9.3E-02 5
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs895953
SETD1B
1.000 0.040 12 121811142 intron variant G/T snv 0.76 5
rs9411378
ABO
9 133270015 intron variant A/C;T snv 5
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs10876041
DIP2B
12 50508099 intron variant T/C snv 0.58 4
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 4
rs11079810
SKAP1
17 48150484 intron variant C/T snv 0.16 4
rs11652146
ZNF652
17 49345001 intron variant G/A;C snv 4
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 4
rs11870935
KPNB1
17 47655239 intron variant G/A;C snv 4
rs150641967
HAPLN4
19 19259532 intron variant AGAC/-;AGACAGAC delins 4
rs1565228
BDNF-AS
11 27564889 intron variant G/A;C snv 4
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 4