Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 5
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs10455025
TSLP
1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 3
rs1046295
PHF11 ; SETDB2-PHF11
1.000 0.080 13 49528674 3 prime UTR variant G/A snv 0.50 0.48 1
rs1047266
TNFRSF10B
1.000 0.080 8 23043188 missense variant G/A;T snv 9.7E-02; 8.0E-06 1
rs10478040
CAMK4
1.000 0.080 5 111254701 intron variant C/T snv 4.8E-02 1
rs10485681 1.000 0.080 20 41864432 intergenic variant A/G snv 8.8E-02 1
rs104893908
NR3C1
0.925 0.160 5 143295561 missense variant T/A snv 2
rs104893909
NR3C1
0.925 0.160 5 143300556 missense variant A/T snv 2
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1048990
PSMA6
0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 8
rs10494132
CHIA
0.851 0.080 1 111289601 upstream gene variant T/C snv 0.26 4
rs1050153
TFRC
0.925 0.120 3 196049444 3 prime UTR variant G/A snv 2
rs1050501
FCGR2B
0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs1050592
CX3CR1
1.000 0.080 3 39265293 3 prime UTR variant A/G snv 0.22 1
rs10507391
ALOX5AP
0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs10508372 1.000 0.080 10 8930055 intergenic variant G/A snv 0.14 1
rs10515807
LOC101927790 ; ADRA1B
1.000 0.080 5 159937991 intron variant G/A snv 0.14 1
rs10515922 1.000 0.080 2 102298194 regulatory region variant A/G snv 6.9E-02 1
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs10519067
RORA
0.925 0.120 15 60776148 intron variant G/A snv 0.20 3
rs10519068
RORA
0.925 0.120 15 60776505 intron variant G/A snv 0.22 2
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1054609
ZPBP2
0.925 0.160 17 39877024 3 prime UTR variant A/C snv 0.40 2