Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs72550870
MASP2
0.776 0.360 1 11046609 missense variant T/C snv 2.1E-02 2.2E-02 1
rs1040441824
PTS
0.882 0.200 11 112233502 missense variant A/G snv 2.1E-05 1
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 4
rs121913675
MET
0.925 0.080 7 116778953 missense variant C/T snv 1
rs121913677
MET
0.925 0.080 7 116783402 missense variant A/G snv 1
rs121913676
MET
0.925 0.080 7 116783421 missense variant G/A;C;T snv 1
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 4
rs567116808
MTUS1
1.000 0.080 8 17646137 missense variant T/C snv 3.0E-04 2.0E-04 1
rs351855
FGFR4
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 1
rs187103704
MTUS1
1.000 0.080 8 17713220 missense variant T/G snv 6.3E-04 2.6E-04 1
rs1057519922
NFE2L2
0.790 0.200 2 177234082 missense variant C/G;T snv 1
rs61733703
MTUS1
1.000 0.080 8 17755585 stop gained G/A;T snv 1.6E-05; 2.4E-03 1
rs1057519925
PIK3CA
0.683 0.560 3 179210291 missense variant G/A;C snv 1
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 5
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 1
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 4
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 3
rs121913281
PIK3CA
0.623 0.520 3 179234296 missense variant C/T snv 1
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 7
rs761113892
HTATIP2
1.000 0.080 11 20376622 missense variant G/A;T snv 8.0E-06; 4.0E-06 1
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 1
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 2
rs121913385
CDKN2A
0.763 0.240 9 21971112 missense variant G/A;C snv 1