Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1154454
ADH7
0.925 0.120 4 99417185 intron variant A/G snv 0.22 2
rs11689011
EPAS1
1.000 0.120 2 46314037 intron variant T/A;C;G snv 2
rs11762213
MET
0.925 0.120 7 116699228 synonymous variant G/A snv 3.3E-02 3.3E-02 2
rs11813268 0.925 0.120 10 103922538 upstream gene variant C/T snv 0.31 2
rs121913669
MET
0.925 0.120 7 116782027 missense variant G/A;T snv 4.0E-06 2
rs1259293
FSTL1
0.925 0.120 3 120421014 intron variant T/C snv 0.59 2
rs12617313
EPAS1
0.925 0.120 2 46332637 intron variant A/G;T snv 2
rs1417080 0.925 0.120 9 79515946 non coding transcript exon variant T/C snv 0.35 2
rs1449964136
MITF
0.925 0.120 3 69936725 start lost G/A snv 8.0E-06 7.0E-06 2
rs1802074
EPDR1 ; SFRP4
0.925 0.120 7 37907501 missense variant C/T snv 0.20 0.24 2
rs2050462
CSF1
0.925 0.120 1 109930334 3 prime UTR variant T/A;G snv 2
rs2241261
RHOBTB2
0.925 0.120 8 23019226 3 prime UTR variant C/G;T snv 2
rs2243270
IL4
0.925 0.120 5 132678417 intron variant A/G;T snv 2
rs2291599
DKK3
0.925 0.120 11 11968352 intron variant T/C snv 0.83 0.85 2
rs2499707
GRM4
0.925 0.120 6 34085889 intron variant T/A;C snv 2
rs2504106
DAAM2
0.925 0.120 6 39854343 intron variant A/G snv 0.61 2
rs2761016
ALAD
0.925 0.120 9 113391072 intron variant T/C snv 0.59 2
rs3118523 0.925 0.120 9 134443675 downstream gene variant G/A snv 0.75 2
rs333951
CSF1
0.925 0.120 1 109909068 upstream gene variant T/C snv 0.74 2
rs35073794
TERC
0.925 0.120 3 169764347 downstream gene variant G/A snv 1.4E-02 2
rs375129361
BAP1
0.925 0.120 3 52408056 missense variant T/A;C snv 4.1E-06 2
rs3889728
AGT
1.000 0.120 1 230713085 intron variant C/T snv 0.24 2
rs4381241
FAF1
0.925 0.120 1 50441766 intron variant T/C snv 0.51 2
rs448012
FLT4
0.925 0.120 5 180619344 missense variant G/C snv 0.63 0.61 2
rs4765623
SCARB1
0.925 0.120 12 124836304 intron variant C/T snv 0.38 2