Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894194
AIP
0.925 11 67483198 stop gained C/T snv 2.8E-05 2.1E-05 4
rs10505476
PCAT1 ; POU5F1B ; CASC8
8 127395871 intron variant C/T snv 0.38 3
rs778826879
MAPK3
16 30121948 missense variant C/G;T snv 1.2E-05; 8.0E-06 3
rs142287570
GCM2
1.000 6 10874335 missense variant T/G snv 6.6E-04 4.9E-04 2
rs146462069
IGSF1
X 131278706 missense variant T/C;G snv 3.8E-05; 9.5E-03 2
rs371918069
GCM2
1.000 6 10874372 missense variant C/T snv 5.6E-05 5.6E-05 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
rs142163070
GML ; CYP11B1
8 142877100 missense variant T/C snv 2.0E-04 4.5E-04 1
rs2227999
XPC
3 14158408 missense variant C/T snv 4.2E-02 4.0E-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
rs763539313
GAPDH
12 6537702 missense variant A/G snv 2.0E-05 4.9E-05 1
rs774679649
CRP
1 159713878 missense variant T/C snv 4.0E-06 7.0E-06 1
rs939481814
UGT1A1 ; UGT1A5 ; UGT1A9 ; UGT1A3 ; UGT1A6 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A4
2 233767063 synonymous variant A/T snv 1
rs4925386
LAMA5
0.776 0.080 20 62345988 intron variant T/C snv 0.56 14
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 11
rs386352319
KCNJ5
0.827 0.080 11 128911724 missense variant G/A;C snv 8
rs121908874
TSHR ; LOC101928462
0.807 0.080 14 81143584 missense variant T/C snv 7
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs10808555
PCAT1 ; POU5F1B ; CASC8
0.925 0.080 8 127397266 intron variant G/A snv 0.65 6
rs386352352
PRKACA
0.851 0.080 19 14097604 missense variant A/C snv 6
rs61734277
GCM2
0.882 0.080 6 10874672 missense variant A/C snv 9.1E-03 8.6E-03 5