Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112417755
GATA3
1.000 0.080 10 8073738 splice acceptor variant G/C;T snv 1
rs12137135 0.925 0.080 1 22348728 intergenic variant A/C;G snv 2
rs12917114 0.925 0.080 15 47852953 intron variant C/T snv 8.9E-02 2
rs730947 0.925 0.080 2 218838575 upstream gene variant A/C snv 1.0E-01 2
rs77113398 0.925 0.080 13 106451558 intergenic variant G/A snv 6.0E-03 2
rs10404257
ACTN4
0.925 0.080 19 38645846 upstream gene variant G/A snv 0.50 2
rs7583877
AFF3
0.925 0.080 2 99844192 intron variant C/T snv 0.61 2
rs370819889
ALB
0.925 0.080 4 73416353 missense variant C/A;T snv 8.0E-06; 9.6E-05 2
rs11089781
APOL3
0.925 0.080 22 36160720 stop gained G/A snv 1.6E-02 6.5E-02 2
rs6936632
CD2AP
0.925 0.080 6 47588297 intron variant G/A snv 7.6E-02 2
rs9349417
CD2AP
0.925 0.080 6 47612921 intron variant A/G snv 0.27 2
rs9369717
CD2AP
0.925 0.080 6 47586732 intron variant T/G snv 0.22 2
rs281874682
COL4A5
0.925 0.080 X 108598805 missense variant C/A;T snv 5.5E-06 2
rs7918972
CUBN
0.925 0.080 10 16828293 intron variant T/G snv 0.15 2
rs904520404
DCDC2
0.925 0.080 6 24302010 stop gained G/A;C snv 4.0E-06; 4.0E-06 2
rs4714384
EDN1
0.925 0.080 6 12297620 downstream gene variant T/C snv 0.45 2
rs2391335
EFNB2
0.925 0.080 13 106519637 non coding transcript exon variant T/C;G snv 0.50 2
rs7490924
EFNB2
0.925 0.080 13 106519396 non coding transcript exon variant A/G snv 0.51 2
rs374118649
FLNB
0.925 0.080 3 58097965 missense variant A/G;T snv 3.6E-05 2
rs373971520
GNG7
0.925 0.080 19 2568808 intron variant CA/-;CACA delins 2
rs1516792
IL1A
0.925 0.080 2 112778356 intron variant G/A snv 2
rs16347
IL1A
0.925 0.080 2 112774138 3 prime UTR variant -/TGAA delins 0.70 2
rs10137082
IL25
0.925 0.080 14 23370824 upstream gene variant C/T snv 0.23 2
rs752390951
KLK4
0.925 0.080 19 50908408 missense variant G/T snv 8.0E-06 7.0E-06 2
rs760452842
KLK4
0.925 0.080 19 50906983 missense variant T/G snv 4.0E-06 2