Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 2
rs10049390
SLCO2A1
0.776 0.080 3 133982275 intron variant G/A snv 0.67 10
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 18
rs10152518 0.790 0.080 15 67884824 intergenic variant G/A;T snv 9
rs10203853
MROH2A
1.000 0.080 2 233778772 intron variant A/G;T snv 2
rs1023890 1.000 0.080 4 117780291 intergenic variant G/A;C snv 1
rs1028166
TENM3 ; TENM3-AS1
0.790 0.080 4 181892145 intron variant G/A snv 0.74 9
rs10318
GREM1
0.882 0.080 15 32733778 3 prime UTR variant C/T snv 0.16 1
rs1035209 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 9
rs10411210
RHPN2
0.742 0.160 19 33041394 intron variant C/T snv 0.22 10
rs10414971
ZNF442
1.000 0.080 19 12351131 missense variant G/A snv 1.9E-03 7.8E-03 1
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 3
rs1043397364
DPEP1
1.000 0.080 16 89637349 missense variant G/A;T snv 2.8E-05; 4.0E-06 1
rs10457678
ECT2L
0.790 0.080 6 138801103 intron variant A/G snv 0.19 10
rs1047781
LOC105447645 ; FUT2
0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 2
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 35
rs104893751
OGG1
0.882 0.240 3 9750423 missense variant G/A;C snv 2.2E-03; 4.0E-06 1
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 37
rs1050152
SLC22A4 ; MIR3936HG
0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 2
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 9
rs10511330
ZBTB20
0.776 0.080 3 114402172 intron variant T/C snv 0.22 10
rs1051424
RPS6KB1
0.925 0.080 17 59946963 3 prime UTR variant A/G snv 0.15 1
rs1057517457
MUTYH
0.851 0.120 1 45332804 frameshift variant GCCAGCCCAG/- delins 7.0E-06 2
rs1057519365
BRIP1
0.851 0.320 17 61780931 frameshift variant TT/- delins 5