Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8905
PRKAR1A ; FAM20A
0.925 0.080 17 68531661 3 prime UTR variant T/A;G snv 2
rs1967327
PRKRA ; PJVK
0.925 0.080 2 178449632 intron variant G/A;C;T snv 2
rs11923427
RAF1
0.925 0.080 3 12622336 intron variant C/G;T snv 2
rs757128066
RIN1
0.925 0.080 11 66334745 missense variant C/A;T snv 6.9E-06; 5.5E-05 2
rs764986276
SHMT1
0.925 0.080 17 18333172 missense variant C/G;T snv 4.0E-06; 4.4E-05 2
rs1425164489
TCN2
0.925 0.080 22 30617374 missense variant A/G;T snv 4.0E-06 2
rs11832059
VDR
0.925 0.080 12 47879066 missense variant A/C;G snv 4.0E-06; 1.9E-03 2
rs997476 0.882 0.080 4 102620848 downstream gene variant G/T snv 4.3E-02 3
rs4147542
ADH1C ; ADH1B
0.882 0.160 4 99347396 intron variant T/C snv 0.33 3
rs1380087059
APC
0.882 0.160 5 112837749 missense variant G/C snv 4.0E-06 3
rs587781394
APC
0.882 0.160 5 112837812 missense variant G/A;C snv 4.0E-06; 8.0E-06 3
rs2304204
BCL2L12 ; IRF3
0.882 0.160 19 49665763 5 prime UTR variant T/C snv 0.39 3
rs774904310
CDKN2A
0.925 0.080 9 21971055 frameshift variant C/- delins 3
rs2059691
CHROMR ; PRKRA
0.882 0.080 2 178437157 intron variant A/G snv 0.72 3
rs1440032367
COL11A2
0.925 0.080 6 33189169 missense variant G/C snv 7.0E-06 3
rs147198552
CXCR4
0.882 0.080 2 136115450 missense variant C/T snv 1.2E-05 7.0E-06 3
rs4562
ELP5 ; CLDN7
0.925 0.080 17 7260420 missense variant A/G snv 0.65 0.70 3
rs63751701
EPM2AIP1 ; MLH1
0.925 0.080 3 36993663 stop gained G/A;T snv 3
rs11986055
IKBKB
0.882 0.080 8 42277660 intron variant A/C;G snv 3
rs6474387
IKBKB
0.882 0.080 8 42328734 intron variant T/C snv 0.76 3
rs121913538
KRAS
0.882 0.080 12 25245328 missense variant C/A;G snv 3
rs6598964
LIN28A
0.882 0.080 1 26419836 intron variant A/G snv 0.67 3
rs230490
LOC105377621
0.882 0.080 4 102466262 downstream gene variant G/A snv 0.34 3
rs9869263
LOC107986170 ; CLDN1
0.925 0.080 3 190312891 synonymous variant A/C;G;T snv 8.0E-06; 0.83; 4.0E-06 3
rs1057519822
MAP2K1
0.925 0.080 15 66481818 missense variant T/A snv 3