Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs713330
CD44
1.000 0.040 11 35202398 intron variant C/T snv 0.74 3
rs7544735
RNU6ATAC35P
1.000 0.040 1 220825571 intron variant G/A snv 0.22 3
rs767580335
RAF1
1.000 0.040 3 12590826 missense variant T/C;G snv 2.4E-05; 4.0E-06 3
rs7729269
MCC
0.925 0.040 5 113384697 intron variant T/C snv 0.17 3
rs8088980
ZNF407
1.000 0.040 18 74666435 intron variant C/T snv 0.51 3
rs8177248
TF
1.000 0.040 3 133760782 non coding transcript exon variant C/T snv 0.28 3
rs8177253
TF
1.000 0.040 3 133761348 non coding transcript exon variant C/T snv 0.31 3
rs10086987 1.000 0.040 8 47177908 intron variant G/A;C snv 2
rs10484432 1.000 0.040 6 26008648 upstream gene variant G/A snv 0.17 2
rs10484433 1.000 0.040 6 26030264 upstream gene variant C/A snv 9.6E-02 2
rs10484435
H3C2
1.000 0.040 6 26031583 upstream gene variant T/G snv 7.6E-02 2
rs1057520026
FLT3
0.925 0.040 13 28028244 missense variant T/G snv 2
rs10757022
SAXO1
1.000 0.040 9 19023615 intron variant A/G snv 0.51 2
rs10887868
PRXL2A
1.000 0.040 10 80434508 3 prime UTR variant G/A snv 0.34 2
rs11189600
HPS1
1.000 0.040 10 98419517 intron variant C/A;T snv 2
rs11264339 1.000 0.040 1 155168172 downstream gene variant C/T snv 0.56 2
rs11265022 1.000 0.040 1 158542829 downstream gene variant T/A snv 0.21 2
rs11639856
TNRC6A
1.000 0.040 16 24777324 missense variant T/A snv 0.17 0.19 2
rs1171114
PRSS35
1.000 0.040 6 83517927 intron variant T/C snv 0.59 2
rs1178981336
C9orf43
1.000 0.040 9 113424228 frameshift variant -/G delins 7.0E-06 2
rs12094989 1.000 0.040 1 26521895 upstream gene variant C/T snv 0.29 2
rs12529505
AK9
1.000 0.040 6 109625358 intron variant G/A snv 0.20 2
rs13220395 1.000 0.040 6 26055140 downstream gene variant G/A;C snv 2
rs13395354
ACOXL
1.000 0.040 2 110842942 intron variant C/T snv 0.18 2
rs1409568 1.000 0.040 10 118871273 intron variant T/C snv 8.2E-02 2