Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1564801473
KLLN ; PTEN
1.000 0.040 10 87864406 5 prime UTR variant -/C delins 1
rs1564801388
PTEN ; KLLN
1.000 0.040 10 87864353 5 prime UTR variant -/G delins 1
rs34808376 0.925 0.040 7 155456016 intron variant -/GC delins 2
rs13294439 1.000 0.040 9 23358877 intron variant A/C snv 0.32 2
rs1033810883
WNT10B ; WNT1
1.000 0.040 12 48979625 missense variant A/C snv 4.0E-06 1
rs1564950387
DEAF1
1.000 0.040 11 687909 splice donor variant A/C snv 1
rs963968092
EDNRA
0.882 0.120 4 147485844 missense variant A/C;G snv 8.0E-06 3
rs1276388879
POGZ
1.000 0.040 1 151405647 missense variant A/C;G snv 1
rs193024911
SYN2
1.000 0.040 3 12151259 missense variant A/C;G snv 2.0E-05; 1.0E-04 1
rs237897
OXTR ; CAV3
1.000 0.040 3 8766599 intron variant A/C;G snv 1
rs766483232
APBA2
1.000 0.040 15 29114003 missense variant A/C;G snv 4.0E-06; 3.6E-04 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs4646536
CYP27B1
0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 14
rs4906902
GABRB3
0.724 0.200 15 26774621 intron variant A/G snv 0.15 14
rs6269
COMT ; MIR4761
0.827 0.240 22 19962429 5 prime UTR variant A/G snv 0.38 10
rs1390938
SLC18A1
0.807 0.200 8 20179202 missense variant A/G snv 0.71 0.78 7
rs2168351
ST8SIA2
0.851 0.120 15 92440492 intron variant A/G snv 0.33 6
rs2745557
PACERR ; PTGS2
0.807 0.200 1 186680089 intron variant A/G snv 0.83 6