Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799852
TF
3 133756878 synonymous variant C/T snv 0.13 0.11 5
rs8177240
TF
3 133758857 intron variant T/C;G snv 0.29 5
rs116009877 6 25715429 regulatory region variant G/A;T snv 4
rs13191659
LINC00240
6 27033276 intron variant C/G;T snv 4
rs6762719
TF
3 133761973 non coding transcript exon variant A/G snv 0.31 4
rs9990333 3 196100334 intergenic variant C/T snv 0.42 4
rs111722075
CMAHP ; CARMIL1
6 25373818 intron variant C/T snv 0.11 2
rs113507773
LOC105374986
6 26255511 upstream gene variant G/A snv 0.10 2
rs143130997
FIG4
6 109780207 intron variant G/A snv 5.9E-03 2
rs150548770
ESM1 ; LOC102467081
5 55020802 intron variant T/C snv 5.4E-03 2
rs181143083
ZDHHC14
6 157434218 intron variant T/A snv 7.5E-04 2
rs202056061
CARMIL1
6 25494109 intron variant AGTT/- delins 2.8E-02 2
rs2442120
DTWD2
5 118970884 intron variant A/C snv 0.98 2
rs73373322
SEPTIN9
17 77385957 intron variant C/T snv 3.1E-02 2
rs10097946
KCNU1 ; LOC105379375
8 36920273 intron variant C/A snv 1.0E-02 1
rs10101752 8 37125160 intergenic variant G/A snv 1.2E-02 1
rs111991936 7 23289983 regulatory region variant G/A snv 1.1E-02 1
rs116112266
LINC01885
2 107482651 intron variant G/C snv 3.5E-03 1
rs138584487
LARGE1
22 33416876 intron variant G/A;C snv 1
rs140911738
MAPRE1
20 32849813 3 prime UTR variant G/C snv 9.3E-03 1
rs141555380
GAB3
X 154677735 3 prime UTR variant C/T snv 4.2E-02 1
rs144453006
SLC3A2
11 62887212 intron variant G/A snv 3.2E-03 1
rs147477420 11 33988237 TF binding site variant G/A snv 3.2E-03 1
rs17052130
SPRY3
X 155675419 intergenic variant T/C snv 4.0E-02 1
rs184908836
LINC02008
3 82041833 intron variant A/G snv 3.8E-03 1