Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1208135
CCDC181
1 169454860 intron variant A/G;T snv 2
rs1208327
NME7
1 169327626 intron variant C/G;T snv 2
rs1209731
NME7
1 169355555 intron variant T/C;G snv 2
rs16861990
NME7
1 169165889 intron variant A/C snv 5.5E-02 2
rs1894692 1 169498416 non coding transcript exon variant G/A snv 0.98 2
rs2038024
SLC19A2
1.000 0.080 1 169486744 non coding transcript exon variant C/A snv 0.88 2
rs2420372
F5
1 169528818 intron variant A/G snv 0.95 2
rs6427194
F5
1 169511883 downstream gene variant T/A snv 0.91 2
rs6427195
F5
1 169511938 downstream gene variant A/C;T snv 2
rs6427197
F5
1 169531352 intron variant C/A snv 0.92 2
rs6687813 1 169508336 downstream gene variant A/C snv 0.93 2
rs6696217 1 169491488 non coding transcript exon variant A/G snv 0.92 2
rs970740 1 169510736 downstream gene variant C/T snv 0.95 2
rs10746487 1 9278630 intergenic variant T/A;C snv 1
rs10919507 1 170885468 intron variant C/T snv 3.0E-02 1
rs113976843
LINC01681
1 170254627 intron variant T/C snv 8.6E-03 1
rs115063924 1 168741790 intron variant C/A;T snv 6.7E-03 1
rs12120558 1 170366687 downstream gene variant G/A snv 1.2E-02 1
rs12122803
C1orf112
1 169825364 intron variant A/G snv 1.4E-02 1
rs12136148 1 170123530 intergenic variant T/G snv 6.9E-02 1
rs12732487
SYT6
1 114120337 intron variant G/A snv 0.11 1
rs1336472
AK4
1 65230247 3 prime UTR variant G/A snv 0.56 1
rs144405847 1 82342193 intron variant C/T snv 4.9E-02 1
rs145163454
ATP1B1
1 169121510 intron variant T/C snv 1.6E-02 1
rs145470028
C1orf198
1 230850661 intron variant G/T snv 1.4E-02 1