Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10467515 13 52927172 regulatory region variant A/G snv 1.2E-02 1
rs138294113 19 11081053 downstream gene variant C/T snv 0.12 1
rs1638665 10 117414434 regulatory region variant T/C snv 2.9E-02 1
rs16837982 2 154682843 intergenic variant G/T snv 5.5E-02 1
rs16890431 4 14429763 intron variant A/G snv 4.5E-02 1
rs4722172 7 22746913 downstream gene variant G/A snv 0.87 1
rs55784307 14 70034647 downstream gene variant C/A snv 0.16 1
rs62084752 17 68093252 upstream gene variant C/A;G snv 1
rs634138 2 160876023 upstream gene variant C/T snv 2.2E-02 1
rs736088 6 25896941 intergenic variant T/C snv 1.0E-02 1
rs7787478 7 97601785 upstream gene variant T/C snv 0.13 1
rs9356334 6 165000406 intron variant T/G snv 2.6E-02 1
rs9567406 13 44303182 intergenic variant A/G;T snv 0.15 1
rs9596720 13 52924312 regulatory region variant C/T snv 1.5E-02 1
rs1180341
BMP8A ; PPIEL
1 39527136 3 prime UTR variant T/C snv 0.48 1
rs11190074
CNNM1
10 99361961 intron variant A/G snv 8.7E-02 1
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
rs1975514
COL4A1
13 110176544 intron variant T/C;G snv 0.36; 4.0E-06 1
rs12520838
COMMD10
5 116161170 intron variant A/C;G snv 0.10 1
rs7476
CREB3L1
11 46321284 3 prime UTR variant A/C snv 0.46 1
rs2554503
CSMD1
8 3967303 intron variant C/G;T snv 0.12 1
rs2073300
CST8
20 23491044 intron variant T/G snv 7.4E-02 1
rs13290547
DAB2IP
9 121725216 intron variant C/T snv 4.0E-02 1
rs11512640
FEZ1
11 125556427 intron variant G/T snv 7.7E-02 1