Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs728926
KLF12
13 73938985 intron variant C/T snv 0.34 2
rs1733724
LNCAROD
10 52464217 intron variant A/G snv 0.82 2
rs242562
MAPT
1.000 0.040 17 45949373 intron variant G/A snv 0.35 2
rs9436640
NFIA
1 61408005 intron variant T/G snv 0.44 2
rs991014
SETBP1
18 44859921 intron variant C/T snv 0.35 2
rs11848785
SIPA1L1
14 71590638 intron variant G/A snv 0.82 2
rs2242285
SLC25A26 ; LRIG1
3 66381178 intron variant A/C;G snv 2
rs4687718
TKT
3 53248287 intron variant A/G snv 0.75 2
rs7342028
VTI1A
10 112719503 intron variant G/C;T snv 2
rs13195040
ZNF184
1.000 0.040 6 27446145 downstream gene variant A/G snv 9.0E-02 2
rs12039739 1 115790490 regulatory region variant C/T snv 0.28 1
rs13185595 5 154492610 upstream gene variant G/A snv 0.41 1
rs1344852 4 20182314 intergenic variant G/A;C;T snv 1
rs1419856 7 35267372 intergenic variant A/G snv 0.11 1
rs4708832 6 159472905 intron variant G/T snv 0.31 1
rs6968945 7 46601302 intergenic variant C/T snv 0.61 1
rs7132327 12 114943266 intergenic variant T/C snv 0.27 1
rs7771320 6 7502516 upstream gene variant T/C snv 5.4E-02 1
rs7909027
CACNB2
10 18406963 intron variant T/C snv 0.44 1
rs1562782
CAND1.11 ; AMPD3
11 10321164 intron variant A/C;G snv 1
rs3929778
CASC20
20 6479643 intron variant C/T snv 0.84 1
rs7537765
CLCN6
1 11827246 intron variant A/G snv 0.15 0.18 1
rs359466
CPEB4
5 173888863 5 prime UTR variant C/G snv 0.11 1
rs10865879
EXOG
3 38535871 intron variant A/C snv 0.21 1
rs2051211
EXOG
3 38518258 intron variant A/C;G snv 0.23 1