Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11077
POLR1C ; XPO5
0.732 0.320 6 43523209 3 prime UTR variant T/G snv 0.47 14
rs11134527
MIR218-2 ; SLIT3
0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs11187870
NOC3L ; PLCE1
1.000 0.080 10 94328109 3 prime UTR variant G/C snv 6.3E-02 1
rs11203366
PADI4
0.925 0.200 1 17331039 missense variant G/A snv 0.56 0.55 2
rs1126667
ALOX12 ; ALOX12-AS1
0.776 0.280 17 6999441 missense variant A/G snv 0.60 0.62 8
rs1129186
PEX6
1.000 0.080 6 42964464 synonymous variant C/T snv 0.48 0.57 1
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1138272
GSTP1
0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs114673809
MTHFR ; C1orf167
0.882 0.080 1 11787703 3 prime UTR variant G/A snv 5.0E-03 3
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
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs115797771
KLF5
0.807 0.080 13 73064505 intron variant A/C snv 5.8E-02 6
rs11599672
LOC105378438 ; PLCE1
0.925 0.080 10 93993019 regulatory region variant T/G snv 0.21 3
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11677
PLA2G2A
1.000 0.080 1 19975471 3 prime UTR variant G/A snv 9.5E-02 1
rs1170595036
SDHC
1.000 0.080 1 161323623 synonymous variant T/C snv 4.0E-06 1
rs11752942
LINC00951 ; TDRG1
0.882 0.080 6 40354019 intron variant A/G snv 0.46 3
rs1200003171
AKT1
0.882 0.120 14 104775122 missense variant C/A;T snv 8.0E-06 4
rs1200055659
S100A16 ; S100A14
0.851 0.080 1 153614902 missense variant G/A snv 7.0E-06 4
rs1206093523
LOC105377015 ; TGFBR2
1.000 0.080 3 30606915 missense variant C/T snv 9.2E-06 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614