Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs574237 9 133303338 downstream gene variant G/A snv 0.53 1
rs58204830
TC2N
14 91836628 intron variant G/A snv 8.4E-02 1
rs607900
MED22
9 133340381 3 prime UTR variant T/C snv 8.1E-02 1
rs62575992
STKLD1
9 133389365 intron variant C/T snv 6.3E-02 1
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs6708166
LBH
2 30303914 intron variant G/A snv 0.32 2
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 15
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs7135039
VWF
12 6051448 intron variant C/T snv 0.40 1
rs7816579
SCARA5
8 27948298 intron variant A/C;G;T snv 1
rs78490142 9 133238613 intergenic variant T/C snv 1.1E-02 1
rs8176719
ABO
0.925 0.120 9 133257521 frameshift variant -/C ins 0.37 0.35 6
rs9271597 0.925 0.080 6 32623514 upstream gene variant T/A snv 0.39 3
rs9390460
STXBP5
6 147373198 intron variant T/C snv 0.51 3
rs9390461
STXBP5
6 147380081 intron variant A/G snv 0.55 2
rs9399599
STXBP5
6 147382163 intron variant A/T snv 0.51 1
rs9616897 22 50644690 intergenic variant C/A;G snv 2