Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs452159
ADA
1.000 0.040 20 44642461 intron variant G/T snv 0.28 2
rs4822489
SPECC1L-ADORA2A ; ADORA2A ; ADORA2A-AS1
0.925 0.200 22 24437792 intron variant T/G snv 0.48 2
rs6684209
CASQ2
1.000 0.040 1 115707991 intron variant C/T snv 0.17 2
rs6787362
FRMD4B
0.925 0.040 3 69178228 intron variant A/G snv 9.3E-02 2
rs9303504
PRKCA
0.925 0.040 17 66319248 intron variant G/C snv 0.59 2
rs9909004
PRKCA
0.925 0.040 17 66310015 intron variant C/T snv 0.59 2
rs1009388
POMC
1.000 0.040 2 25168232 intron variant G/C snv 0.18 1
rs1544223
ADORA3 ; TMIGD3
1.000 0.040 1 111503935 intron variant C/T snv 0.72 1
rs28714259 0.882 0.120 15 23463380 intergenic variant G/A snv 0.19 5
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 4
rs9351814 0.882 0.040 6 71484004 intergenic variant A/C snv 0.35 4
rs9885413 0.925 0.040 5 110840429 intergenic variant G/T snv 0.19 2
rs73956431
B4GALT6
0.827 0.120 18 31699870 regulatory region variant C/T snv 8.4E-02 6
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs1815739
ACTN3
0.763 0.240 11 66560624 stop gained C/T snv 0.37 17
rs766265889
TTN-AS1 ; TTN
0.827 0.240 2 178535508 stop gained G/A;T snv 8.0E-06; 4.0E-06 11
rs111033560
PLN ; CEP85L
0.807 0.040 6 118559037 stop gained T/G snv 1.6E-05 9
rs767312316
UTS2R
1.000 0.040 17 82375046 stop gained C/A;G;T snv 6.6E-05; 1.7E-05; 1.7E-05 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131