Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1232880706
FBN1
0.689 0.440 15 48526247 stop gained C/A;T snv 36
rs121908525
AGXT
0.790 0.160 2 240875159 missense variant T/C snv 4.4E-05 5.6E-05 7
rs780813696
HNF4A ; MIR3646
0.827 0.240 20 44407388 missense variant C/A;T snv 4.1E-06 7.0E-06 5
rs114368325
CYP24A1
0.925 0.120 20 54158136 missense variant G/A;C snv 6.6E-04; 8.0E-06 4
rs121964880
VAX2 ; ATP6V1B1
0.851 0.280 2 70958113 missense variant T/C snv 4.0E-06 4
rs121908523
AGXT
0.882 0.160 2 240868986 missense variant G/A snv 1.2E-05 4.2E-05 3
rs180177161
AGXT
0.882 0.160 2 240878721 missense variant G/A;C snv 5.9E-06 3
rs180177227
AGXT
0.882 0.160 2 240871406 missense variant G/A;C;T snv 1.8E-05; 1.3E-05 3
rs104893726
CLDN16
0.882 0.200 3 190408416 missense variant T/G snv 3
rs80356708
GRHPR
0.882 0.160 9 37424862 frameshift variant G/- delins 3
rs779588655
SLC12A1
0.882 0.160 15 48234946 frameshift variant T/- delins 8.0E-06 3
rs201304511
SLC34A1
0.882 0.120 5 177387874 splice donor variant G/A snv 7.8E-05 4.2E-05 3
rs145591298
CLDN19
0.925 0.120 1 42735969 missense variant C/T snv 1.1E-05 2.1E-05 2
rs757796926
GRHPR
0.925 0.120 9 37426659 splice region variant G/A snv 4.0E-06 7.0E-06 2
rs1555466999
LOC107984758 ; SLC12A1
0.925 0.120 15 48244876 missense variant G/A snv 2
rs896545456
LOC112267905 ; SLC12A1
0.925 0.120 15 48229233 missense variant G/A snv 7.0E-06 2
rs201331677
SLC34A1
0.925 0.120 5 177398090 missense variant C/T snv 3.2E-05 2.8E-05 2
rs376131751
SLC34A1
0.925 0.120 5 177396762 missense variant G/C snv 2.8E-05 1.7E-04 2
rs778000327
SLC3A1
0.925 0.120 2 44280877 frameshift variant G/- del 2.7E-04 2
rs142772770
SLC34A1
1.000 0.120 5 177387765 missense variant T/C snv 1.6E-05 1.4E-05 1