Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs10931936
CASP8
0.827 0.120 2 201279205 intron variant T/C snv 0.72 6
rs11051196
TSPAN11
12 30980130 intron variant C/T snv 0.27 1
rs11065756
CCDC63
0.925 0.080 12 110900990 intron variant C/T snv 6.1E-02 3
rs11065783
LOC105369980 ; LINC01405
12 110958445 non coding transcript exon variant A/G snv 1.9E-02 1
rs11066015
ACAD10
0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 5
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs11187842
PLCE1
0.925 0.080 10 94292754 intron variant C/T snv 7.8E-02 5
rs11254327
CUBN
10 17006709 intron variant C/T snv 0.40 1
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs11473
BSG
0.882 0.080 19 582982 3 prime UTR variant C/A;T snv 4
rs11548103
S100A14
0.882 0.080 1 153615864 splice region variant C/T snv 0.40 0.39 4
rs115510139
COL6A3
0.827 0.120 2 237331726 intron variant A/T snv 0.60 6
rs11552822
CDKN2A
1.000 9 21971109 missense variant C/A;T snv 4.3E-06 2
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22 13
rs11776675
CDH17
8 94163787 intron variant T/C snv 0.23 1
rs11843987
TFDP1
13 113589954 intron variant A/G snv 9.1E-02 1
rs11898821
FLACC1
2 201334965 intron variant T/C snv 0.46 1
rs11972901 7 85966605 intergenic variant A/G snv 0.47 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614