Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2721
LOC105375591 ; INSIG1
1.000 0.080 7 155296033 non coding transcript exon variant T/G snv 0.85 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs5351
EDNRB-AS1 ; EDNRB
0.807 0.240 13 77901178 synonymous variant T/C;G snv 0.57 7
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 7
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 7
rs33931746
HBB
0.807 0.280 11 5227099 5 prime UTR variant T/C;G snv 6
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs183433761
GCG ; LOC101929532
0.851 0.200 2 162152278 5 prime UTR variant T/C;G snv 5
rs33981098
HBB
0.827 0.280 11 5227102 5 prime UTR variant T/C;G snv 5
rs939348
THRA
0.851 0.240 17 40075600 intron variant T/C;G snv 5
rs1801058
GRK4
0.882 0.120 4 3037423 missense variant T/C;G snv 0.62 4
rs762403278
MTHFR
0.851 0.200 1 11796244 missense variant T/C;G snv 1.6E-05; 4.0E-06 4
rs1422753499
MMP12
0.925 0.120 11 102873034 missense variant T/C;G snv 7.0E-06 2
rs2302870
KLF7
0.925 0.120 2 207088682 intron variant T/C;G snv 2
rs297325
SOX6
0.925 0.120 11 16368048 intron variant T/C;G snv 2
rs1127568
ADCY3
1.000 0.080 2 24823221 synonymous variant T/C;G snv 0.69; 4.0E-06 1
rs185218834
SSTR4
1.000 0.080 20 23036294 missense variant T/C;G snv 4.0E-06; 3.5E-04 1
rs267606994
PYY
1.000 0.080 17 43953299 missense variant T/C;G snv 8.2E-06 1
rs7379701 1.000 0.080 5 71715685 upstream gene variant T/C;G snv 1
rs9939506
TOX3
1.000 0.080 16 52494395 intron variant T/C;G snv 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77