Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000283
HSD11B1 ; HSD11B1-AS1
0.925 0.080 1 209721316 intron variant G/A snv 0.18 2
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs10033652
RASGEF1B
1.000 0.040 4 81571913 intron variant C/T snv 0.62 1
rs1003880422
TH
0.925 0.080 11 2166716 missense variant G/A;T snv 6.9E-06 2
rs10052957
NR3C1
0.851 0.160 5 143407136 non coding transcript exon variant G/A snv 0.28 4
rs1007888
MIF-AS1
0.882 0.120 22 23898914 non coding transcript exon variant C/T snv 0.46 4
rs10085637
LOC107986824 ; PDK4
1.000 0.040 7 95596501 5 prime UTR variant T/C;G snv 0.40 1
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 8
rs10185316
LOC107985940 ; INSIG2
1.000 0.040 2 118086902 upstream gene variant C/G snv 0.32 1
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs10247649
PDK4
0.925 0.080 7 95586935 non coding transcript exon variant A/G snv 0.43 2
rs1040288
NR3C2
1.000 0.040 4 148126966 intron variant G/C snv 0.49 3
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1044250
ANGPTL4
0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 12
rs10484092
FRMD6-AS2 ; FRMD6
1.000 0.040 14 51489516 intron variant A/G snv 4.8E-02 2
rs10488698
BUD13
1.000 0.040 11 116763231 missense variant G/A snv 6.4E-02 4.8E-02 2
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs1049673
CD36
0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 7
rs10499859
CD36
0.925 0.120 7 80629494 intron variant A/G snv 0.46 2
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 8
rs1051295
KCNB1 ; LOC105372649
0.925 0.080 20 49372368 3 prime UTR variant A/G snv 0.22 3
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19