Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 6
rs9370867
MYLIP
0.827 0.120 6 16145094 missense variant A/G snv 0.60 0.63 7
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 9
rs9289231
KALRN
0.827 0.120 3 124055231 intergenic variant T/G snv 0.15 5
rs915014
C1orf167 ; MTHFR
0.925 0.040 1 11789412 missense variant T/C snv 2
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs879254925
MIR6886 ; LDLR
0.790 0.120 19 11113680 missense variant G/T snv 8
rs879254850
MIR6886 ; LDLR
0.776 0.160 19 11113365 missense variant A/G;T snv 4.0E-06 9
rs879254840
LDLR ; MIR6886
0.827 0.120 19 11113322 missense variant A/G snv 5
rs879254693
LDLR
0.807 0.160 19 11107424 missense variant T/A;C;G snv 7
rs879254582
LDLR
0.851 0.160 19 11105488 frameshift variant AGCCCCT/- delins 4
rs877087
RYR3
0.882 0.080 15 33582074 intron variant T/C;G snv 4
rs867186
PROCR ; MMP24-AS1-EDEM2
0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 15
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs8070488
HGS
0.882 0.080 17 81696901 synonymous variant T/C snv 0.21 0.26 3
rs8042271 0.882 0.040 15 89030987 intergenic variant G/A;T snv 3
rs80356814
LMNA
0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs797044485
LMNA
0.851 0.160 1 156134832 missense variant G/A snv 4
rs79681911
SAA1
0.882 0.040 11 18269755 missense variant G/A snv 2.1E-03 8.0E-04 3
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs7895340
TCF7L2
0.851 0.160 10 113041766 intron variant G/A snv 0.53 4
rs7833904 0.882 0.040 8 58505103 upstream gene variant A/T snv 0.55 3
rs774887459
SGSM3
0.882 0.080 22 40405776 missense variant G/A snv 4.0E-06 4
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14