Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs189107782
FRG1-DT
4 189807855 intron variant C/T snv 1.5E-03 1
rs2023844
HOTTIP
7 27203619 intron variant G/A snv 0.93 1
rs2338796
FBXL20
17 39399374 intron variant A/G snv 0.27 1
rs2601006
CCT2 ; MIR3913-1
12 69585737 5 prime UTR variant C/T snv 0.39 1
rs34823645
C2orf83
2 227647210 intron variant T/C snv 3.9E-04 1
rs35311980 2 228295484 intergenic variant C/T snv 4.9E-05 1
rs35483183
COL4A4
2 227011971 intron variant G/A snv 8.4E-02 1
rs35572189
MIR3186 ; BAHCC1
17 81451999 missense variant G/A;C snv 0.34 1
rs35924503 2 228266570 intergenic variant T/C snv 1.5E-04 1
rs3759794
LTK
15 41514460 upstream gene variant G/A snv 0.12 1
rs3805382
NMU
4 55605384 intron variant A/G snv 0.36 0.29 1
rs4109437
FRG1-DT
4 189848068 intron variant G/A;C snv 1
rs4288924 14 68835682 intergenic variant G/A;T snv 1
rs4738817
CHD7
8 60708054 intron variant G/A snv 0.36 1
rs539606836
CUBN
10 16963744 intron variant G/A snv 1.7E-04 1
rs55798132
LOC105377785
8 2808621 intron variant G/A;T snv 1
rs6712846 2 207024356 intergenic variant G/A snv 0.53 1
rs6750228
NRXN1 ; LOC730100
2 51084986 intron variant T/A snv 6.9E-02 1
rs6768627
MYL3
3 46853886 intron variant C/T snv 0.13 1
rs7654754
SHROOM3
4 76488642 intron variant G/A snv 0.43 1
rs7670121
NR3C2
4 148207444 intron variant A/G snv 0.24 1
rs7731168
CWC27
5 65000644 intron variant G/C snv 0.29 1
rs8035855
MAPKBP1
15 41785763 intron variant G/A snv 0.59 1
rs838142
FUT1 ; IZUMO1
19 48748894 3 prime UTR variant A/G snv 0.39 1
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13