Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs36217263
KL
1.000 0.040 13 33015697 upstream gene variant A/- del 0.21 4
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs3755166
LRP2
1.000 0.080 2 169363371 upstream gene variant A/C;G snv 4
rs2070665
APOA1 ; APOA1-AS
11 116836968 intron variant A/C;G snv 0.85 2
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs4743763
ABCA1
1.000 0.040 9 104830901 intron variant A/C;T snv 0.36 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs1265538677
CPB2-AS1 ; CPB2
0.790 0.200 13 46055808 synonymous variant A/G snv 4.0E-06 10
rs780092
GCKR
0.827 0.160 2 27520287 intron variant A/G snv 0.18 10
rs5030717
TLR4
0.807 0.240 9 117711556 intron variant A/G snv 0.13 9
rs1984112
CD36
0.807 0.280 7 80613604 intron variant A/G snv 0.33 8
rs2106809
ACE2
0.827 0.120 X 15599938 intron variant A/G snv 0.19 8
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs9370867
MYLIP
0.827 0.120 6 16145094 missense variant A/G snv 0.60 0.63 7
rs5072
APOA1 ; APOA1-AS
11 116836867 intron variant A/G snv 0.89 5