Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7141987
MIR329-2 ; MIR323A ; MIR329-1 ; MIR758 ; MEG8 ; MIR1197
0.925 0.080 14 101025887 intron variant T/C snv 0.58 2
rs17749155
MSRA
0.925 0.080 8 10210563 intron variant G/A snv 0.16 2
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs3127075
CASP7
1.000 0.080 10 113712354 intron variant G/A;C snv 1
rs1247942 0.925 0.080 12 114235918 downstream gene variant G/A;C snv 2
rs10108511
LINC00208
0.925 0.080 8 11578007 non coding transcript exon variant T/A;C snv 2
rs2188554
ASZ1 ; CFTR
1.000 0.080 7 117400063 intron variant A/G snv 0.20 1
rs17451754
CFTR
0.925 0.080 7 117616658 intron variant G/A snv 0.10 2
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4740363
ABL1
1.000 0.080 9 130753797 intron variant A/G snv 7.8E-02 1
rs17002540 1.000 0.080 X 140863896 intergenic variant C/T snv 0.20 1
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 28
rs17708574
PDGFRB
1.000 0.080 5 150141675 intron variant G/A snv 8.2E-02 1
rs2341926 0.925 0.080 2 150927414 intergenic variant A/G snv 0.20 2
rs12465911 0.925 0.080 2 150929228 intergenic variant C/T snv 0.21 2
rs13396805 0.925 0.080 2 150964998 intergenic variant C/T snv 0.20 2
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs4661636
CASP9
0.925 0.160 1 15496566 intron variant C/T snv 0.24 2
rs7632500
LOC107986152
0.925 0.080 3 168007561 downstream gene variant A/G snv 0.17 5
rs9823696 0.925 0.080 3 184065565 downstream gene variant A/G;T snv 2
rs10419226
CRTC1
0.925 0.080 19 18692362 intron variant T/G snv 0.67 5
rs199620551
CRTC1
0.925 0.080 19 18693485 intron variant G/- del 9.2E-02 2
rs1035142
FLACC1
0.807 0.200 2 201288355 3 prime UTR variant T/C;G snv 0.54 7
rs7255
GDF7
0.925 0.080 2 20679060 3 prime UTR variant T/A;C snv 3