Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17368528
H6PD
0.827 0.400 1 9264154 missense variant C/A;T snv 0.12 8.9E-02 5
rs11808092
EVI5
1.000 0.080 1 92607671 missense variant C/A snv 0.20 0.20 1
rs11804321
EVI5
1.000 0.080 1 92543756 intron variant T/C snv 0.13 1
rs41286801
EVI5
1.000 0.080 1 92509907 3 prime UTR variant C/T snv 0.11 1
rs6689470
GFI1
1.000 0.080 1 92485653 intron variant G/A snv 0.14 1
rs6662618 0.882 0.200 1 92469854 downstream gene variant T/G snv 0.75 3
rs17519972
GLMN ; RPAP2
1.000 0.080 1 92362948 intron variant A/C snv 0.15 2
rs1411751
GPC5
0.925 0.120 13 92245255 intron variant G/A snv 0.16 2
rs10492503
GPC5
1.000 0.080 13 92232844 intron variant T/A snv 0.36 1
rs12694
BTG1 ; LOC101928617 ; LOC107984023
1.000 0.080 12 92145814 5 prime UTR variant T/C snv 0.46 1
rs731652
BTG1 ; LOC101928617
1.000 0.080 12 92145033 intron variant G/A snv 0.16 1
rs1109670
LOC105373414 ; LOC105373416
1.000 0.080 2 9109909 upstream gene variant C/A;G snv 1
rs290986
SYK
1.000 0.080 9 90801254 upstream gene variant A/G snv 0.18 2
rs11609
IQGAP1
1.000 0.080 15 90500533 3 prime UTR variant C/G snv 0.42 2
rs8042861
IQGAP1
1.000 0.080 15 90434101 intron variant G/A;T snv 1
rs12212193
BACH2
0.925 0.280 6 90287050 intron variant A/G snv 0.38 2
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs11755527
BACH2
0.851 0.360 6 90248512 intron variant C/G snv 0.36 5
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 6
rs1805008
MC1R
0.732 0.240 16 89919736 missense variant C/T snv 4.7E-02 4.8E-02 16
rs1805755
KLRG1 ; M6PR
1.000 0.080 12 8949816 upstream gene variant A/C;G snv 1.7E-02 1
rs879181391
MIR6766 ; POLG
1.000 0.080 15 89328774 missense variant T/C snv 1
rs2234978
FAS
1.000 0.080 10 89012072 synonymous variant T/C snv 0.77 0.72 1
rs7538427
GTF2B
1.000 0.080 1 88873739 intron variant C/T snv 0.93 2
rs305217
PKN2
1.000 0.080 1 88754789 intron variant G/A snv 8.6E-02 2