Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042852
CBLB
1.000 0.080 3 105658671 3 prime UTR variant C/G;T snv 1
rs1059292
SLC3A2 ; SNORD29 ; SNORD25 ; SNHG1 ; SNORD30 ; SNORD28 ; SNORD27 ; SNORD26
1.000 0.080 11 62855579 non coding transcript exon variant T/C snv 7.2E-02 9.0E-02 1
rs10878232 1.000 0.080 12 65128867 intergenic variant T/A;C;G snv 1
rs10981694
LOC107987119 ; SLC31A1
1.000 0.080 9 113224129 intron variant T/G snv 8.7E-02 1
rs11045585
SLCO1B3-SLCO1B7 ; SLCO1B3
1.000 0.080 12 20892760 intron variant A/G snv 0.17 1
rs11071938
SMAD3
1.000 0.080 15 67127649 intron variant C/T snv 0.27 1
rs11574852
NFKB2
1.000 0.080 10 102401718 intron variant A/C snv 2.3E-02 2.3E-02 1
rs11713419
IL5RA
1.000 0.080 3 3108583 5 prime UTR variant A/G snv 0.19 1
rs117512489
PLB1
1.000 0.080 2 28620281 missense variant G/A snv 2.0E-02 1.2E-02 1
rs12000445 1.000 0.080 9 23426273 intron variant A/G snv 0.18 1
rs121913430
EGFR
1.000 0.080 7 55174740 missense variant G/A snv 1
rs1228223399
CYP1B1-AS1 ; CYP1B1
1.000 0.080 2 38075045 missense variant G/A snv 5.0E-06 1
rs1252688154
MUC1
1.000 0.080 1 155187520 missense variant C/T snv 4.0E-06 1
rs12614710
EPAS1
1.000 0.080 2 46337952 intron variant T/G snv 0.69 1
rs12621220 1.000 0.080 2 112840678 non coding transcript exon variant C/T snv 0.24 1
rs12686377
LOC107987119 ; SLC31A1
1.000 0.080 9 113241753 intron variant C/A;T snv 1
rs12728900
LIN28A
1.000 0.080 1 26420316 intron variant G/A snv 0.29 1
rs1273957629
TSC2
1.000 0.080 16 2076130 missense variant G/A;T snv 4.0E-06 1
rs12806698
RRM1
1.000 0.080 11 4094744 non coding transcript exon variant C/A snv 0.22 1
rs12949918
STAT3
1.000 0.080 17 42374255 intron variant T/C snv 0.39 1
rs1301481068
CBL
1.000 0.080 11 119232532 missense variant C/T snv 4.0E-06 1
rs13173911
CCDC127
1.000 0.080 5 214298 non coding transcript exon variant C/T snv 0.38 1
rs13213007
HDAC2
1.000 0.080 6 113961317 intron variant G/A snv 0.22 1
rs1343232776
LOC107985874 ; EML4
1.000 0.080 2 42295429 missense variant G/A snv 4.0E-06 1
rs1405937
CASP3 ; PRIMPOL
1.000 0.080 4 184650784 intron variant G/C snv 0.29 1