Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3753584
MTHFR ; CLCN6
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 10
rs12108497
PRIMPOL ; CASP3
0.851 0.080 4 184650403 intron variant C/G;T snv 6
rs1760893
TEP1
0.807 0.080 14 20412501 intron variant C/A snv 0.89 6
rs10817938
PTCSC2
0.882 0.080 9 97700127 non coding transcript exon variant T/C snv 3.2E-02 5
rs12800438
NADSYN1
1.000 0.080 11 71459957 non coding transcript exon variant G/A;T snv 5
rs2143571
SAMM50
0.827 0.080 22 43995806 intron variant G/A snv 0.25 5
rs2299939
PTEN
0.827 0.080 10 87897393 intron variant C/A;T snv 5
rs3131003
PSORS1C1
0.925 0.080 6 31125705 5 prime UTR variant G/A snv 0.52 5
rs3807992
CAV1
0.925 0.080 7 116557191 intron variant G/A snv 0.28 5
rs621559
CFAP57 ; LOC105378685 ; EBNA1BP2
0.827 0.080 1 43179740 intron variant G/A snv 0.18 5
rs9267673
C2 ; CYP21A2
0.925 0.080 6 31915902 intron variant C/A;T snv 0.12 5
rs1200055659
S100A16 ; S100A14
0.851 0.080 1 153614902 missense variant G/A snv 7.0E-06 4
rs1234220
PTEN
0.851 0.080 10 87885716 intron variant A/G snv 9.1E-02 4
rs2069852 0.925 0.080 7 22732641 downstream gene variant G/A;C snv 4
rs2890658
CD274
0.925 0.080 9 5465130 intron variant C/A;T snv 4
rs4663402
ATG16L1
0.851 0.080 2 233285017 intron variant A/T snv 5.1E-02 4
rs6588147
LEPR
0.851 0.080 1 65469811 intron variant G/A snv 0.70 4
rs80309960
XRCC5
0.851 0.080 2 216122110 missense variant T/A snv 3.5E-04 1.1E-03 4
rs10485505
ITCH
1.000 0.080 20 34437762 intron variant C/G;T snv 3
rs10519613
IL15
1.000 0.080 4 141732931 3 prime UTR variant C/A snv 0.10 3
rs10836347
CD44
1.000 0.080 11 35231586 3 prime UTR variant C/T snv 0.11 3
rs11564475
CTNNB1
0.882 0.080 3 41238542 intron variant A/G snv 3.7E-02 3
rs121913676
MET
0.925 0.080 7 116783421 missense variant G/A;C;T snv 3
rs157077
GSTO2
1.000 0.080 10 104278136 intron variant T/C snv 0.45 0.53 3
rs17006625
KAT2B
0.925 0.080 3 20119604 missense variant A/C;G snv 4.0E-06; 3.3E-02 3