Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4846044
C1orf167-AS1 ; C1orf167
1 11779941 missense variant T/C;G snv 0.95 2
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs2013208
RBM5 ; RBM6
3 50091966 intron variant C/T snv 0.61 0.56 4
rs235314
PTTG1IP
21 44851537 missense variant C/T snv 0.48 0.46 3
rs7599598
FER1L5
2 96686103 missense variant A/G;T snv 0.41 2
rs2071449
HOXC4 ; HOXC5 ; MIR615
12 54034227 intron variant C/A;T snv 0.35; 4.2E-06 4
rs35866622
MAMSTR
19 48714803 splice region variant C/T snv 0.34 0.32 3
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs10935070
TOPBP1
3 133623144 missense variant T/C;G snv 0.29; 4.0E-06 1
rs2269238
PGM1
1 63651866 intron variant G/A;T snv 3.2E-05; 0.24 1
rs1107413
SRPRB ; LOC105374116
3 133805873 missense variant G/C snv 0.22 0.20 1
rs8294
PGM1
1 63659697 3 prime UTR variant C/T snv 0.21 0.17 1
rs34311866
TMEM175
0.882 0.080 4 958159 missense variant T/C snv 0.18 0.14 6
rs66476925
DNAH11 ; LOC105375183
7 21571781 intron variant G/A;C;T snv 4.4E-06; 0.17; 4.4E-06 3
rs1049296
TF
0.882 0.120 3 133775510 missense variant C/T snv 0.16 0.14 4
rs1799852
TF
3 133756878 synonymous variant C/T snv 0.13 0.11 5
rs12561919
C1orf167 ; C1orf167-AS1
1.000 0.040 1 11779866 missense variant C/T snv 0.13 0.13 3
rs13284665
ZER1
9 128751091 intron variant A/G snv 0.11 0.10 2
rs11102001
GSTM5 ; EPS8L3
0.925 0.080 1 109757069 missense variant G/A snv 9.4E-02 0.16 4
rs1799899
TF
1.000 0.080 3 133756968 missense variant G/A snv 5.2E-02 4.5E-02 2
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs72640211
C1orf167-AS1 ; C1orf167
1 11778705 synonymous variant G/A snv 4.4E-02 4.8E-02 1
rs41266779
H4C1
6 26021644 upstream gene variant C/T snv 4.0E-02 4.3E-02 2
rs117222687
COMT ; ARVCF
22 19968491 intron variant G/C snv 3.8E-02 4.1E-02 2