Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11655838
LOC339166
17 5819886 intron variant A/G snv 0.46 1
rs1181835738
ACE
17 63490971 missense variant A/G snv 4.0E-06 7.0E-06 1
rs12122803
C1orf112
1 169825364 intron variant A/G snv 1.4E-02 1
rs12675621
NUGGC
8 28040935 intron variant A/G snv 0.40 1
rs1336708
FGF14 ; FGF14-IT1 ; LOC107984615
13 102312653 intron variant A/G snv 0.28 1
rs138916004
LEMD3
12 65188408 intron variant A/G snv 4.1E-03 1
rs1423386 5 62689026 intergenic variant A/G snv 0.19 1
rs1558519
VWF
12 6044572 intron variant A/G snv 0.40 1
rs181813804 11 48706704 intergenic variant A/G snv 8.1E-03 1
rs191436110 1 170621629 intron variant A/G snv 3.0E-03 1
rs192874339 11 49397227 intergenic variant A/G snv 7.6E-03 1
rs2028385 12 96423644 intron variant A/G snv 0.19 1
rs2288073
FAM228A
2 24190429 missense variant A/G snv 0.26 0.25 1
rs2321744
LOC107984589
13 34032049 intergenic variant A/G snv 0.14 1
rs2710201
LOC102723686
7 153227808 intergenic variant A/G snv 0.22 1
rs2901092
SLC19A2
1 169487155 non coding transcript exon variant A/G snv 4.7E-02 1
rs3087505
KLKB1
4 186258332 3 prime UTR variant A/G snv 0.91 1
rs3176891
ENTPD1-AS1 ; ENTPD1
10 95821187 intron variant A/G snv 0.50 1
rs3211752
F10
13 113133145 intron variant A/G snv 0.41 1
rs35352631
LOC102724680
12 84943333 upstream gene variant A/G snv 3.2E-02 1
rs3804476
LY86
6 6625471 intron variant A/G snv 0.34 1
rs380904
ZC3H3
8 143483735 intron variant A/G snv 0.72 1
rs409169
LINC00299
2 8415954 intron variant A/G snv 0.17 1
rs4507975
PAPPA2
1 176715296 intron variant A/G snv 0.32 1
rs536477
CHRM3
1 239882608 intron variant A/G snv 0.49 1