Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs814698
ZNF618
1.000 0.080 9 113967563 intron variant A/T snv 0.22 2
rs1749824
ZMIZ1
0.925 0.080 10 79164105 intron variant C/A snv 0.39 3
rs60236946
ZAR1L
1.000 0.080 13 32309059 intron variant C/T snv 1.7E-02 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs491567
WDR72
1.000 0.080 15 53654396 intron variant A/C snv 0.34 4
rs17730281
WDR72
1.000 0.080 15 53615751 missense variant G/A snv 0.26 0.22 3
rs690346
WDR72
1.000 0.080 15 53716648 missense variant T/C snv 0.99 0.96 1
rs10794720
WDR37
1.000 0.080 10 1110225 intron variant T/C snv 0.89 4
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs4293393
UMOD
0.827 0.200 16 20353266 intron variant A/G snv 0.20 8
rs13329952
UMOD
1.000 0.080 16 20355185 intron variant T/C snv 0.24 3
rs183962941
UMOD
0.925 0.080 16 20343125 intron variant G/A snv 1.1E-02 2
rs201761378
UMOD
1.000 0.080 16 20341292 missense variant C/T snv 9.7E-04 2.4E-04 1
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 7
rs2727040
TRIM49B
1.000 0.080 11 49036051 intron variant T/A;C snv 2
rs7708392
TNIP1
0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs3803800
TNFSF13 ; TNFSF12-TNFSF13
0.807 0.240 17 7559652 missense variant A/G snv 0.70 0.64 7
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 23
rs174528
TMEM258 ; MYRF
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 5