Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11575542
FIGNL1 ; DDC
7 50463289 missense variant C/T snv 2.3E-02 5.5E-02 1
rs1168357
GRIP1
12 66356099 intron variant T/C snv 0.50 1
rs2030712
HIPK2 ; LOC105375530
7 139610185 intron variant C/A;T snv 1
rs751772105
KCNJ11
11 17387362 missense variant C/A;T snv 4.0E-05 1
rs6581768
LOC105369816
12 67683408 intergenic variant A/G snv 0.25 1
rs6428106
LOC105371664
1 192585301 intron variant G/T snv 0.14 1
rs1423621991
MMP1 ; WTAPP1
11 102796745 missense variant C/T snv 1
rs1001030257
PDE4D
5 58988559 missense variant T/C snv 2.0E-05 2.1E-05 1
rs1290773788
PDE4D
5 58989799 missense variant C/T snv 1
rs1455341183
PDE4D
5 59038945 missense variant C/T snv 1
rs6865647
PDE4D
5 59103374 intron variant A/G;T snv 1
rs770069803
PDE4D
5 58977286 missense variant C/G snv 4.0E-06 1
rs996876302
PECAM1
17 64363155 missense variant C/T snv 3.5E-05 1
rs375411329
PPARG
3 12379746 missense variant A/G snv 7.0E-06 1
rs1300938986
PTGS1
9 122392516 missense variant C/T snv 4.0E-06 1
rs1009840
SGK1 ; LOC107986646
6 134225547 intron variant G/A snv 0.53 1
rs316029
SLC22A2
6 160265636 intron variant T/C snv 0.89 1
rs9658625
SOAT2
12 53103618 missense variant A/G snv 9.3E-02 7.4E-02 1
rs1419367513
SOD2 ; ACAT2 ; SOD2-OT1
6 159762678 non coding transcript exon variant G/A snv 1
rs1232013698
TNF
6 31577208 missense variant G/T snv 4.1E-06 1
rs1564858
TNFRSF11B
8 118932927 splice region variant G/A snv 0.11 9.9E-02 1
rs1156619081
UCP3
11 74005787 missense variant T/C snv 4.0E-06 1
rs1318525693
UCP3
11 74006370 missense variant C/G;T snv 1
rs10178409 1.000 0.080 2 73628380 downstream gene variant G/T snv 0.26 2
rs1066621 1.000 0.080 3 191708066 regulatory region variant C/T snv 0.39 2