Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs937283
MDM2
0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs751402
ERCC5 ; BIVM-ERCC5
0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs1256046734
LEPR
0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 12
rs3846662
HMGCR
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 12
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
rs6059655
RALY
0.790 0.080 20 34077942 intron variant A/G snv 0.95 10
rs3087386
REV1
0.790 0.160 2 99439044 missense variant A/G snv 0.58 0.61 8
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 3
rs1340420
TNKS2
0.925 0.080 10 91857549 intron variant A/G snv 0.71 0.70 3
rs2071230
WTAPP1 ; MMP1
0.882 0.080 11 102790228 3 prime UTR variant A/G snv 0.15 3
rs2847281
PTPN2
1.000 0.040 18 12821594 intron variant A/G snv 0.32 3
rs121913082
FAS
1.000 0.040 10 89014205 missense variant A/G snv 2
rs121913083
FAS
1.000 0.040 10 89008907 missense variant A/G snv 2
rs6819385
CHRNA9
0.925 0.080 4 40337557 intron variant A/G snv 0.52 2
rs1078305
GSN
1.000 0.040 9 121289122 intron variant A/G snv 0.70 1
rs11707807
LPP
1.000 0.040 3 188370473 intron variant A/G snv 0.36 1
rs6743068
FLACC1
1.000 0.040 2 201289197 intron variant A/G snv 0.72 1
rs2230641
CCNH
0.807 0.240 5 87399457 missense variant A/G;T snv 0.18 0.17 8
rs5491
ICAM1
0.827 0.160 19 10274864 missense variant A/G;T snv 4.0E-06; 2.8E-02 6
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs8063761
DEF8
1.000 0.040 16 89961218 intron variant A/T snv 0.33 1
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs1899663
HOTAIR
0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs987525
CCDC26
0.807 0.160 8 128933908 intron variant C/A snv 0.31 7