Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11788387 9 81855961 regulatory region variant G/T snv 0.14 2
rs149014416 8 29812253 downstream gene variant G/- delins 1.5E-02 2
rs1558001 7 81777764 intergenic variant T/C snv 0.63 2
rs117023642
LINC02153
8 20981609 intron variant C/G snv 1.6E-02 2
rs2001841 3 61513935 intergenic variant G/A snv 0.34 1
rs480745 1 82804287 intron variant G/A snv 6.4E-02 1
rs539974331 1 182336514 downstream gene variant AA/-;A;AAA delins 1.6E-02 1
rs61953951 13 31486393 upstream gene variant G/A snv 8.9E-02 1
rs35113467
C10orf90
10 126538306 intron variant T/C snv 0.18 1
rs687184
LOC107987054 ; LINC01239
9 22725625 intron variant G/A;C snv 1
rs112912841
LPP
3 188269895 intron variant A/G snv 0.12 1
rs2146858
OTX2-AS1
14 57067427 intron variant C/A;T snv 0.44 1
rs3777722
RNASET2
6 166938616 missense variant C/A;G;T snv 0.18; 4.1E-06; 6.6E-05 1
rs737263
SHISAL1
22 44244728 3 prime UTR variant G/A;C snv 1
rs34635471
SLC7A14-AS1
3 170594457 intron variant AA/- del 5.3E-02 1
rs116461311
SLIT2
4 20329377 intron variant A/C;G snv 1
rs1877720
SPATA6
1 48358735 intron variant C/T snv 7.1E-02 1
rs72545460
STK35
20 2163705 intron variant -/C ins 1
rs111873142
TBCD
17 82910808 intron variant C/G;T snv 1
rs140162370
TMEM241
18 23391045 intron variant G/C snv 2.7E-02 1
rs73814923
VGLL4
3 11608090 intron variant C/A;T snv 1