Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs386352319
KCNJ5
0.827 0.080 11 128911724 missense variant G/A;C snv 8
rs7837328
CASC8 ; PCAT1 ; POU5F1B
0.882 0.120 8 127410882 intron variant A/G snv 0.52 8
rs121908874
TSHR ; LOC101928462
0.807 0.080 14 81143584 missense variant T/C snv 7
rs2302615
ODC1-DT ; SNORA80B ; ODC1
0.807 0.120 2 10448012 intron variant C/T snv 0.31 7
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs7968585
LINC02354
0.851 0.160 12 47838310 downstream gene variant C/G;T snv 7
rs1057517457
MUTYH
0.851 0.120 1 45332804 frameshift variant GCCAGCCCAG/- delins 7.0E-06 6
rs10808555
PCAT1 ; POU5F1B ; CASC8
0.925 0.080 8 127397266 intron variant G/A snv 0.65 6
rs121912535
STON1-GTF2A1L ; LHCGR ; GTF2A1L
0.827 0.240 2 48688427 missense variant A/C snv 6
rs386352352
PRKACA
0.851 0.080 19 14097604 missense variant A/C snv 6
rs7131056
DRD2
0.827 0.200 11 113459052 intron variant A/C snv 0.51 6
rs1290398674
GNAS
0.851 0.240 20 58854075 missense variant G/A;T snv 5
rs1535989 0.925 0.080 13 105370372 intergenic variant A/G;T snv 4
rs386352318
KCNJ5
0.925 0.080 11 128911776 missense variant T/G snv 4
rs10505476
PCAT1 ; POU5F1B ; CASC8
8 127395871 intron variant C/T snv 0.38 3
rs2838958
SLC19A1
1.000 0.080 21 45528653 intron variant G/A snv 0.45 3
rs17503908
ATM ; C11orf65
1.000 0.080 11 108344670 intron variant T/G snv 6.7E-02 2
rs4952490
SLC8A1-AS1 ; SLC8A1
1.000 0.080 2 40145564 intron variant A/G snv 0.33 2
rs6586714
NAT1
1.000 8 18216433 intron variant A/G snv 0.84 2
rs1201299
TBL1XR1
3 177053096 intron variant C/T snv 1.7E-02 1
rs2720574
PDGFRL
8 17578682 intron variant C/A;G;T snv 1
rs2855798
KCNJ1 ; LOC107984409
11 128863066 intron variant G/T snv 0.21 1
rs386834263
CACNA1D
3 53673113 missense variant G/C snv 1
rs4648310
PTGS2
1 186671393 downstream gene variant T/C;G snv 1
rs939481814
UGT1A1 ; UGT1A5 ; UGT1A9 ; UGT1A3 ; UGT1A6 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A4
2 233767063 synonymous variant A/T snv 1