Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs755249
PPIEL ; BMP8A
1 39529402 3 prime UTR variant C/A;T snv 5
rs11039100
OR52N2 ; TRIM5
11 5805773 intron variant T/C snv 0.11 2
rs118039278
LPA
6 160564494 intron variant G/A snv 4.3E-02 2
rs2074633
HDAC9
7 18996297 3 prime UTR variant T/A;C snv 2
rs4842266 12 79557786 upstream gene variant G/A snv 0.50 2
rs6668352 1 11854772 downstream gene variant G/A snv 0.24 2
rs9557207
UBAC2
13 99384164 intron variant A/G snv 0.17 2
rs10046574
CNOT4
7 135485722 intron variant C/T snv 7.4E-02 1
rs10428206
CNTN3
3 74485377 intron variant T/C snv 1.5E-02 1
rs10467515 13 52927172 regulatory region variant A/G snv 1.2E-02 1
rs10484876
PAQR8 ; EFHC1
6 52389351 intron variant C/T snv 0.14 1
rs10979314
LOC105376214
9 108310149 intergenic variant G/A snv 7.2E-02 1
rs11077983
SLC16A3
17 82227312 upstream gene variant C/G;T snv 1
rs11190074
CNNM1
10 99361961 intron variant A/G snv 8.7E-02 1
rs11206019
ZYG11B
1 52794278 intron variant G/T snv 0.16 1
rs11220138
FEZ1 ; STT3A-AS1
11 125585927 intron variant C/T snv 7.7E-02 1
rs11512640
FEZ1
11 125556427 intron variant G/T snv 7.7E-02 1
rs1180341
BMP8A ; PPIEL
1 39527136 3 prime UTR variant T/C snv 0.48 1
rs11819158
GOT1
10 99418299 intron variant G/T snv 2.3E-02 1
rs11942139
PPP2R2C
4 6429357 intron variant T/C snv 2.5E-02 1
rs12257301
OPN4
10 86655778 intron variant G/A snv 7.1E-02 1
rs12335314
NDUFB9 ; MTSS1
8 124550784 intron variant T/G snv 1.7E-02 1
rs12445943
WWOX
16 78775175 intron variant G/A snv 0.17 1
rs12520838
COMMD10
5 116161170 intron variant A/C;G snv 0.10 1
rs13290547
DAB2IP
9 121725216 intron variant C/T snv 4.0E-02 1