Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1190983
EVL
0.925 0.080 14 100031649 intron variant T/C snv 0.61 2
rs1333017606
GPC2 ; STAG3
1.000 0.080 7 100175622 missense variant C/G;T snv 4.0E-06; 8.0E-06 1
rs2273802
WARS1 ; WDR25
0.925 0.080 14 100376562 5 prime UTR variant G/A snv 0.33 2
rs11292
HIF1AN
0.925 0.080 10 100553850 3 prime UTR variant A/G snv 0.22 2
rs144940475
TMTC4
1.000 0.080 13 100612442 missense variant T/C snv 1.4E-04; 8.1E-06 4.1E-04 1
rs17094222 0.925 0.080 10 100635683 intergenic variant T/C snv 0.17 3
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs17024926
NPAS2
0.851 0.120 2 100889540 intron variant T/C snv 0.34 4
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs2305160
NPAS2 ; NPAS2-AS1
0.776 0.200 2 100974842 missense variant A/G snv 0.71 0.75 9
rs4919510
SEMA4G ; MIR608 ; MRPL43
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs11541353
NPAS2-AS1 ; NPAS2
0.851 0.120 2 100977729 missense variant C/T snv 0.14 0.14 4
rs3739008
NPAS2
0.925 0.080 2 100996106 3 prime UTR variant C/T snv 0.24 2
rs1235690743
LZTS2
1.000 0.080 10 101003969 missense variant G/C snv 4.0E-06 7.0E-06 1
rs500760
PGR
0.882 0.120 11 101039260 synonymous variant T/C snv 0.24 0.29 3
rs10895054
PGR
0.925 0.080 11 101039579 intron variant A/T snv 0.11 2
rs1042839
PGR
0.925 0.080 11 101051471 synonymous variant G/A snv 0.13 0.11 2
rs56103835
MIR323B
0.925 0.080 14 101056219 non coding transcript exon variant T/A;C snv 4.0E-06; 0.28 2
rs1293387481
PGR
0.925 0.080 11 101062537 missense variant G/A snv 4.0E-06 7.0E-06 3
rs1042838
PGR
0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 12
rs590688
PGR
0.925 0.080 11 101105243 intron variant C/G snv 0.47 2
rs775092033
PGR ; PGR-AS1
0.925 0.080 11 101127471 missense variant G/C snv 2
rs11571149
PGR ; PGR-AS1
0.925 0.080 11 101127937 missense variant G/T snv 2