Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1447708158
RAF1
1.000 0.120 3 12604160 synonymous variant C/T snv 7.0E-06 1
rs764168570
RAF1
1.000 0.120 3 12608879 synonymous variant C/T snv 7.0E-06 1
rs1335035506
SHMT1
1.000 0.120 17 18340207 missense variant A/G snv 4.0E-06 1.4E-05 1
rs148701087
SHMT1 ; MIR6778
1.000 0.120 17 18340762 missense variant G/A snv 6.4E-04 8.8E-04 1
rs1185926926
SLC19A1
1.000 0.120 21 45531748 missense variant A/G snv 4.1E-06 1
rs1250480918
SLC19A1
1.000 0.120 21 45537803 synonymous variant G/A snv 4.6E-06 1
rs1320767909
SLC19A1
1.000 0.120 21 45531982 missense variant A/G snv 4.1E-06 1
rs2991216
SYK
1.000 0.120 9 90865745 intron variant A/G snv 0.21 1
rs1921310
TANK
1.000 0.120 2 161192690 intron variant A/G snv 0.15 1
rs2582869
TNFSF13B
1.000 0.120 13 108259797 intron variant A/G;T snv 1
rs13178127
XRCC4
1.000 0.120 5 83293613 intron variant A/G snv 3.3E-02 1
rs10008492 1.000 0.120 4 38764099 intergenic variant C/G;T snv 2
rs207186 0.925 0.120 1 55359252 intron variant C/T snv 7.7E-03 2
rs61733010
AKR1A1
0.925 0.120 1 45561805 missense variant C/G;T snv 4.0E-06; 4.3E-04 1.9E-03 2
rs3813729
C1RL ; C1R
0.925 0.120 12 7089608 missense variant C/G;T snv 2
rs13113
CASP8
0.925 0.200 2 201287439 3 prime UTR variant T/A snv 0.33 2
rs4661636
CASP9
0.925 0.160 1 15496566 intron variant C/T snv 0.24 2
rs1801181
CBS
0.925 0.160 21 43060506 synonymous variant G/A snv 0.33 2
rs234706
CBS
0.925 0.160 21 43065240 synonymous variant G/A snv 0.27 2
rs2855429
COL11A2
0.925 0.120 6 33190412 intron variant A/C snv 0.78 2
rs606231364
FAS
0.925 0.160 10 89003071 missense variant G/A snv 2
rs12211228
IRF4
1.000 0.120 6 408833 3 prime UTR variant G/C snv 0.11 2
rs3789068
MIR4435-2HG ; BCL2L11
0.925 0.120 2 111151670 intron variant A/G snv 0.41 2
rs161870
MTRR
0.925 0.160 5 7878079 synonymous variant T/C snv 0.18 0.21 2
rs758837678
NBN ; DECR1
0.925 0.120 8 90001503 missense variant C/T snv 2