Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1799895
SOD3
0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799998
CYP11B2
0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 13
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800730
HFE ; LOC108783645
0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs1800779
NOS3
0.763 0.320 7 150992855 intron variant G/A;C snv 9
rs1800888
ADRB2
0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs1801252
ADRB1
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805126
SCN5A
0.925 0.040 3 38550915 synonymous variant A/G snv 0.39 0.44 2
rs1805127
KCNE1
0.732 0.240 21 34449523 missense variant T/C snv 0.64 2.0E-04 17
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1815739
ACTN3
0.763 0.240 11 66560624 stop gained C/T snv 0.37 17
rs1860561
ATP2A2
0.851 0.080 12 110345436 intron variant G/A snv 0.19 5
rs198358
NPPA-AS1 ; CLCN6
0.925 0.040 1 11844019 3 prime UTR variant T/C snv 0.32 4
rs200432861
PKHD1
1.000 0.040 6 51775844 missense variant G/A;C snv 2.4E-05; 2.0E-05 1
rs200536955
HSPB6 ; PROSER3
0.925 0.040 19 35756980 missense variant G/A;T snv 7.0E-04 3
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2073440
HDC
0.851 0.200 15 50242317 missense variant T/G snv 3.4E-02 5.9E-02 4