Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11190140
NKX2-3 ; LINC01475
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 6
rs4409764 0.925 0.040 10 99524480 upstream gene variant T/A;G snv 3
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs9557207
UBAC2
13 99384164 intron variant A/G snv 0.17 2
rs9557195
GPR183 ; UBAC2
13 99304368 intron variant T/C snv 0.16 1
rs3742130
GPR18 ; UBAC2
0.925 0.040 13 99255087 synonymous variant G/A snv 0.16 0.16 3
rs9297145
KPNA7
0.827 0.120 7 99161494 intergenic variant C/A snv 0.67 6
rs2395022
KPNA7
7 99152756 intergenic variant A/C snv 0.93 1
rs2297322
SLC15A1
1.000 0.040 13 98723927 missense variant C/G;T snv 0.22 4
rs1363907
ERAP2 ; ERAP1
1.000 0.040 5 96917099 intron variant G/A snv 0.38 2
rs26653
ERAP1
0.882 0.080 5 96803547 missense variant C/A;G;T snv 0.64; 8.0E-06; 9.1E-04 4
rs483905
MAML2
1.000 0.040 11 96290263 intron variant G/A snv 0.26 2
rs62561366 1.000 0.040 9 95555669 intergenic variant A/T snv 3.9E-02 2
rs3765534
ABCC4
0.882 0.200 13 95163161 missense variant C/T snv 2.3E-02 1.2E-02 4
rs145080284 1.000 0.080 10 94662973 intergenic variant C/G snv 2.8E-02 2
rs11187157 10 92742487 TF binding site variant T/C snv 0.40 1
rs7911264 10 92677094 intergenic variant T/A;C;G snv 1
rs34856868
BTBD8
1 92088726 missense variant G/A snv 2.0E-02 2.0E-02 1
rs4743820
LINC00484 ; LOC100507103
1.000 0.040 9 91166134 non coding transcript exon variant C/T snv 0.61 2
rs7165170
CRTC3-AS1 ; CRTC3
1.000 0.040 15 90638257 non coding transcript exon variant A/C snv 0.26 2
rs7495132
CRTC3 ; CRTC3-AS1
0.790 0.080 15 90629669 intron variant C/T snv 0.12 10
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 7
rs7015630 1.000 0.040 8 89863690 intergenic variant T/A;C snv 2
rs12035735
LRRC8D
1 89839786 intron variant G/A snv 1.4E-03 4
rs304496
LIPA
10 89387005 intron variant A/G snv 0.96 1