Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4148325
UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A1 ; UGT1A9 ; UGT1A3 ; UGT1A4 ; UGT1A6
0.851 0.080 2 233764663 intron variant C/T snv 0.36 11
rs7001819
LOC105379243
0.925 0.080 8 11792966 upstream gene variant T/C snv 0.35 4
rs121913564
MC4R
0.882 0.080 18 60371403 missense variant A/C snv 2.0E-05 1.4E-05 3
rs757139012
SIM1
0.882 0.080 6 100390522 missense variant T/C snv 8.0E-06; 4.0E-06 1.4E-05 3
rs1064891
PFKFB3
0.925 0.080 10 6234611 3 prime UTR variant T/C snv 0.37 2
rs121913566
MC4R
0.925 0.080 18 60372165 missense variant T/C snv 4.0E-06 2
rs1322837244
QPCTL
0.925 0.080 19 45698622 missense variant C/T snv 2
rs13447331
MC4R
0.925 0.080 18 60371970 missense variant G/A snv 1.7E-04 7.7E-05 2
rs1800571
PPARG
0.925 0.080 3 12381349 missense variant C/A snv 1.4E-05 2
rs201408477
POMC
0.925 0.080 2 25161455 missense variant A/G snv 1.8E-04 1.6E-04 2
rs540467809
QPCTL
0.925 0.080 19 45698838 missense variant A/G snv 1.0E-03 2.2E-04 2
rs564343
PACS1
0.925 0.080 11 66127695 intron variant A/G snv 0.46 2
rs6020846
CTNNBL1
0.925 0.080 20 37777265 intron variant A/G snv 0.13 2
rs746906443
MC4R
0.925 0.080 18 60371868 missense variant A/G snv 4.0E-06 2
rs750845408
LOC101929710 ; PCSK1
0.925 0.080 5 96423317 missense variant T/C snv 4.5E-05 7.0E-05 2
rs917346005
CADM2
0.925 0.080 3 85912502 missense variant A/G snv 2
rs10487818
NAMPT
1.000 0.080 7 106269615 intron variant A/T snv 1.1E-02 1
rs1800949
ENPP1
1.000 0.080 6 131807424 upstream gene variant C/G;T snv 0.18 1
rs768916374
MC4R
1.000 0.080 18 60371880 missense variant T/G snv 4.0E-06 1
rs9932411
FTO
1.000 0.080 16 53971251 intron variant C/T snv 0.50 1
rs587777230
PIGX ; CEP19
0.851 0.120 3 196707811 stop gained G/A snv 2.1E-05 4
rs2076349
LAMB3
0.882 0.120 1 209626885 missense variant C/T snv 0.13 0.13 3
rs2239607
ACACB
0.925 0.120 12 109209475 intron variant A/G snv 0.14 3
rs943003
ENPP1
0.882 0.120 6 131819872 non coding transcript exon variant C/T snv 0.64 3
rs199951903
ND6 ; CYTB
0.925 0.120 MT 15497 missense variant G/A snv 2