Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs56848936
SYMPK
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 11
rs6022999
CYP24A1
0.790 0.160 20 54171474 intron variant A/G snv 0.36 9
rs4809960
CYP24A1
0.807 0.240 20 54169534 intron variant T/C snv 0.20 8
rs2302615
ODC1-DT ; SNORA80B ; ODC1
0.807 0.120 2 10448012 intron variant C/T snv 0.31 7
rs4464148
SMAD7
0.827 0.120 18 48932662 intron variant T/C snv 0.25 7
rs2270916
CASR
0.851 0.120 3 122282252 intron variant T/C snv 0.13 0.11 6
rs60745952
LOC107986195 ; LOC105377481
0.925 0.080 4 148827842 intron variant T/C snv 0.13 6
rs6918698
CCN2
0.851 0.200 6 131952117 intron variant G/A;C snv 5
rs9365723
SYNJ2
0.827 0.080 6 158014540 intron variant A/C;G snv 0.56 5
rs10222633
CASR
0.925 0.080 3 122258079 intron variant G/A snv 0.45 4
rs10934578
CASR
0.925 0.080 3 122258435 intron variant G/T snv 0.30 4
rs11721827
TLR3
0.851 0.200 4 186069983 intron variant A/C snv 0.12 4
rs12591359
MIR4713HG ; CYP19A1
0.925 0.080 15 51247171 intron variant G/A snv 0.41 4
rs1902432
PCAT1 ; LOC105375751
0.851 0.120 8 127012566 intron variant A/G snv 0.25 4
rs2736118
TERT
0.882 0.120 5 1260080 intron variant T/C snv 0.33 4
rs2870820
MDM2
0.851 0.120 12 68808546 intron variant C/T snv 0.30 4
rs3804513
IL17A
0.851 0.080 6 52188399 intron variant A/T snv 2.4E-02 4
rs6588147
LEPR
0.851 0.080 1 65469811 intron variant G/A snv 0.70 4
rs7987649
FLT1
0.925 0.080 13 28320278 intron variant A/G snv 0.35 4
rs11986055
IKBKB
0.882 0.080 8 42277660 intron variant A/C;G snv 3
rs2059691
CHROMR ; PRKRA
0.882 0.080 2 178437157 intron variant A/G snv 0.72 3
rs2189517
RAD51B
0.882 0.080 14 68536271 intron variant A/G snv 0.49 3
rs352144
TLR9
0.925 0.080 3 52227452 intron variant T/G snv 3.7E-02 3
rs4147542
ADH1C ; ADH1B
0.882 0.160 4 99347396 intron variant T/C snv 0.33 3
rs4648110
NFKB1 ; LOC105377347
0.925 0.080 4 102612664 intron variant T/A snv 0.22 3