Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11780263
SCARA5
8 27966315 intron variant G/A snv 0.19 1
rs6708166
LBH
2 30303914 intron variant G/A snv 0.32 2
rs9271597 0.925 0.080 6 32623514 upstream gene variant T/A snv 0.39 3
rs137631 22 39321701 upstream gene variant T/C snv 0.92 1
rs1869365
RAB5C
17 42141847 intron variant T/C snv 0.40 2
rs9616897 22 50644690 intergenic variant C/A;G snv 2
rs10102164
RP1
8 54509054 upstream gene variant G/A snv 0.19 4
rs57040304
VWF
12 5953728 non coding transcript exon variant A/G snv 9.7E-02 1
rs12423482
VWF
12 5961679 intron variant A/G snv 4.4E-02 1
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs2238109
VWF
12 6044801 intron variant T/A snv 0.40 2
rs11064010
VWF
12 6050980 intron variant T/A;C snv 2
rs7135039
VWF
12 6051448 intron variant C/T snv 0.40 1
rs548630 5 73110832 intergenic variant A/C;T snv 2
rs10498631
TC2N
14 91802187 intron variant C/T snv 0.29 1
rs58204830
TC2N
14 91836628 intron variant G/A snv 8.4E-02 1
rs4904820
TC2N
14 91852591 intron variant G/A snv 0.53 2