Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9919007 1.000 0.040 9 133244140 intergenic variant C/T snv 0.27 2
rs9411471 1.000 0.040 9 133244704 intergenic variant G/A snv 0.27 2
rs7855466 0.925 0.080 9 133245916 downstream gene variant C/T snv 0.23 3
rs7046863 1.000 0.040 9 133246054 downstream gene variant T/C snv 0.27 1
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs11558538
LOC107985948 ; HNMT
0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 19
rs10105842 1.000 0.040 8 142590254 intergenic variant C/T snv 0.15 1
rs9324593 1.000 0.040 8 142605634 intergenic variant A/G snv 0.18 1
rs28473387 1.000 0.040 8 142626112 intergenic variant T/C snv 0.63 1
rs9297976
JRK ; PSCA
0.790 0.160 8 142670817 intron variant T/C;G snv 7
rs2920283
JRK ; PSCA
0.925 0.040 8 142675619 intron variant T/C snv 0.44 2
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 28
rs2976391
PSCA ; JRK
0.790 0.160 8 142681306 intron variant C/A;G snv 0.42; 2.5E-04 7
rs2976392
JRK ; PSCA
0.724 0.240 8 142681514 3 prime UTR variant G/A snv 0.46 0.45 15
rs2920297
PSCA ; JRK
1.000 0.040 8 142681665 3 prime UTR variant A/G snv 0.44 1
rs138377917
PSCA
0.827 0.160 8 142682113 stop gained G/A snv 2.1E-02 2.2E-02 5
rs1045574
PSCA
1.000 0.040 8 142682540 3 prime UTR variant G/A snv 0.46 0.44 1
rs12155758 0.882 0.080 8 142684467 upstream gene variant G/A snv 0.23 3
rs2244163
LY6K ; LNCOC1
1.000 0.040 8 142703082 3 prime UTR variant T/G snv 0.42 0.43 1
rs2164308
LY6K ; LNCOC1
1.000 0.040 8 142704241 3 prime UTR variant C/T snv 0.49 1
rs2572904
LNCOC1
1.000 0.040 8 142710775 intron variant A/C snv 0.49 1
rs2585140
LNCOC1 ; THEM6
1.000 0.040 8 142725478 intron variant A/G snv 0.51 1
rs1036385 1.000 0.040 8 142761483 upstream gene variant T/C;G snv 1
rs2572925
LY6D
1.000 0.040 8 142786489 missense variant C/G;T snv 0.36 1