Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs775646772
XDH
1.000 0.080 2 31366061 stop gained G/A;C snv 1.6E-05; 1.2E-05 1
rs1379560430
XBP1
1.000 0.080 22 28795637 missense variant C/T snv 4.0E-06 1
rs1346044
WRN
0.708 0.440 8 31167138 missense variant T/C snv 0.24 0.23 23
rs1801195
WRN
0.776 0.240 8 31141764 missense variant G/A;T snv 8.0E-06; 0.45 0.46 8
rs2230009
WRN
0.827 0.240 8 31064419 missense variant G/A snv 5.8E-02 7.8E-02 5
rs188554751
WRN
0.851 0.200 8 31120403 missense variant C/T snv 4.0E-06 4
rs3087425
WRN
0.882 0.160 8 31120294 missense variant C/T snv 2.8E-03 8.7E-04 3
rs2287499
WRAP53 ; TP53
0.925 0.080 17 7688850 missense variant C/G;T snv 0.20 4
rs1533767
WNT11
0.851 0.120 11 76194756 splice region variant G/A snv 0.27 0.23 5
rs11643870
WFDC1
1.000 0.080 16 84318346 missense variant G/A snv 8.8E-03 8.4E-03 1
rs5758550
WBP2NL
0.925 0.080 22 42016707 intron variant G/A;T snv 2
rs4919682
WBP1L
0.925 0.080 10 102824573 intron variant C/G;T snv 0.24 2
rs2273802
WARS1 ; WDR25
0.925 0.080 14 100376562 5 prime UTR variant G/A snv 0.33 2
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 16
rs12241008
VTI1A
0.716 0.160 10 112520943 intron variant T/C snv 0.13 16
rs11196067
VTI1A
0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 9
rs10754339
VTCN1
0.882 0.120 1 117147650 3 prime UTR variant G/A snv 0.88 0.76 3
rs10801935
VTCN1
0.925 0.080 1 117179265 intron variant C/A;G snv 2
rs3738414
VTCN1
0.925 0.080 1 117210906 5 prime UTR variant G/A;T snv 3.8E-02 2
rs1182821166
VPS72 ; TMOD4
1.000 0.080 1 151176787 missense variant T/C snv 1
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42