Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000879
VIL1
2 218439407 intron variant G/A snv 4.1E-02 3
rs1002487
RPS6KA1
1 26539480 intron variant T/C snv 5.3E-02 1
rs10033119
NPY1R
4 163324702 3 prime UTR variant A/G snv 7.9E-02 1
rs10047459
APOA1-AS ; SIK3
11 116851110 intron variant C/T snv 0.80 1
rs10047462
APOA1-AS ; SIK3
11 116851325 intron variant G/C;T snv 3
rs10054063 5 173965395 downstream gene variant A/T snv 0.26 4
rs10055011
CERT1
5 75502331 intron variant G/A snv 0.12 1
rs1009360
LOC107984063 ; LINC02245 ; LINC02576
2 65048915 intron variant T/C snv 0.51 2
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 8
rs10101067
EYA1
8 71495139 intron variant G/C snv 6.2E-02 2
rs10105606 8 19970337 downstream gene variant C/A snv 0.42 2
rs10106652 1.000 0.040 8 20070649 intergenic variant G/A snv 0.29 3
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4
rs10118611
BNC2
9 16597467 intron variant G/A snv 3.0E-02 1
rs10119
TOMM40
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 5
rs10120653
RXRA
9 134415237 intron variant G/T snv 1.2E-02 3
rs10125024
RXRA
9 134407131 intron variant C/T snv 1.5E-02 1
rs10127775
GALNT2
1 230160042 intron variant A/G;T snv 4
rs10138032
HIF1A ; HIF1A-AS3
14 61717464 intron variant A/G snv 8.8E-02 1
rs10152811
AGBL1 ; AGBL1-AS1
15 86311359 intron variant A/C snv 0.28 1
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 7
rs10198175 0.925 0.080 2 20934123 intergenic variant A/G snv 0.93 3