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
rs10019888 4 26061368 regulatory region variant A/G snv 0.17 3
rs10054063 5 173965395 downstream gene variant A/T snv 0.26 4
rs10087900 8 143221248 downstream gene variant G/A snv 0.37 1
rs10091038 8 29502788 intergenic variant A/C snv 0.57 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
rs10099160
LPL
8 19964304 intron variant T/G snv 0.20 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
rs10107815
MSRA
8 10156645 intron variant G/C snv 5.1E-02 4
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4
rs10120087
ABCA1
9 104898869 intron variant C/A;T snv 2
rs10120653
RXRA
9 134415237 intron variant G/T snv 1.2E-02 3
rs10127775
GALNT2
1 230160042 intron variant A/G;T snv 4
rs10149080
GCH1
14 54889676 intron variant C/T snv 4.4E-02 2
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
rs10198423 2 85333439 upstream gene variant G/A;C;T snv 1
rs10200587
BMPR2
2 202554561 intron variant A/G snv 7.0E-03 2
rs10212938
LOC107986321 ; NPY2R
4 155207180 non coding transcript exon variant T/C snv 2.6E-02 2
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs10239940
BAZ1B
7 73487060 intron variant A/T snv 2.6E-02 2
rs1026422 7 50280211 upstream gene variant G/A snv 0.51 1
rs10271556
NAMPT
7 106258428 intron variant C/T snv 5.6E-02 4