Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs58204830
TC2N
14 91836628 intron variant G/A snv 8.4E-02 1
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs150926226
TMLHE ; TMLHE-AS1
X 155491696 intron variant G/A;C snv 1
rs3124758
SLC2A6
9 133479731 upstream gene variant G/A;C snv 1
rs551924 9 133306143 downstream gene variant G/A;C snv 1
rs9271597 0.925 0.080 6 32623514 upstream gene variant T/A snv 0.39 3
rs2238109
VWF
12 6044801 intron variant T/A snv 0.40 2
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs11064010
VWF
12 6050980 intron variant T/A;C snv 2
rs9390460
STXBP5
6 147373198 intron variant T/C snv 0.51 3
rs1869365
RAB5C
17 42141847 intron variant T/C snv 0.40 2
rs137631 22 39321701 upstream gene variant T/C snv 0.92 1
rs2723889
STAB2
12 103606692 intron variant T/C snv 0.72 1
rs607900
MED22
9 133340381 3 prime UTR variant T/C snv 8.1E-02 1
rs78490142 9 133238613 intergenic variant T/C snv 1.1E-02 1
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs1070073
STAB2
12 103606541 intron variant T/G snv 0.71 2