Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2897075
ZKSCAN1
1.000 0.040 7 100032719 intron variant C/T snv 0.31 1
rs7079679
PKD2L1
1.000 0.040 10 100295789 intron variant C/A snv 0.57 1
rs2278843
PKD2L1
1.000 0.040 10 100296751 intron variant A/G snv 0.58 1
rs12692398
CYS1
0.925 0.080 2 10060189 intron variant G/A snv 0.17 2
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs138886989
RPL36A-HNRNPH2 ; GLA
0.925 0.160 X 101401763 missense variant T/C snv 1.9E-04 2.8E-05 2
rs56386186
WDR20
1.000 0.040 14 102193651 intron variant T/C snv 9.7E-02 2
rs2071230
WTAPP1 ; MMP1
0.882 0.080 11 102790228 3 prime UTR variant A/G snv 0.15 3
rs773474756
MMP1 ; WTAPP1
0.925 0.080 11 102790467 missense variant T/C snv 8.1E-06 2
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs470234
WTAPP1
1.000 0.040 11 102811075 intron variant T/A;G snv 2
rs470928
WTAPP1
1.000 0.040 11 102814649 intron variant G/A;T snv 2
rs470292
WTAPP1
1.000 0.040 11 102814664 intron variant C/A snv 0.90 2
rs505987
WTAPP1
1.000 0.040 11 102815179 intron variant A/G snv 0.89 2
rs475937
WTAPP1
1.000 0.040 11 102816969 intron variant A/C;T snv 2
rs520146
WTAPP1
1.000 0.040 11 102819400 intron variant T/C snv 0.90 2
rs564018
WTAPP1
0.925 0.080 11 102820688 intron variant A/G;T snv 3
rs688258
WTAPP1
1.000 0.040 11 102821364 intron variant A/C;T snv 2
rs595128
WTAPP1
1.000 0.040 11 102822378 intron variant T/C snv 0.90 2
rs499459
WTAPP1
0.925 0.080 11 102822455 intron variant A/G snv 0.90 3
rs611705
WTAPP1
1.000 0.040 11 102823737 intron variant C/T snv 0.90 2
rs473238
WTAPP1
1.000 0.040 11 102829629 intron variant T/C snv 0.90 2
rs553542
WTAPP1
1.000 0.040 11 102830645 intron variant C/T snv 0.90 2
rs525119
WTAPP1
1.000 0.040 11 102831415 intron variant G/T snv 0.90 2
rs646760
WTAPP1
1.000 0.040 11 102832547 non coding transcript exon variant A/T snv 0.10 2