Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11624704
NRXN3
1.000 0.080 14 78319734 intron variant A/C snv 0.13 3
rs121913564
MC4R
0.882 0.080 18 60371403 missense variant A/C snv 2.0E-05 1.4E-05 3
rs1457489 1.000 0.080 18 60194728 upstream gene variant G/A snv 0.29 3
rs1553548194
SCN1A-AS1 ; SCN1A
1.000 0.080 2 166048938 inframe deletion AAT/- delins 3
rs164147
NOS1AP
0.882 0.080 1 162368607 3 prime UTR variant A/C snv 0.76 3
rs17381664
ZZZ3
1.000 0.080 1 77582646 intron variant T/C snv 0.29 3
rs17817288
FTO
1.000 0.080 16 53773852 intron variant A/C;G snv 3
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 3
rs2272127
IL18RAP
1.000 0.080 2 102423413 intron variant C/G snv 0.22 3
rs2289277
TSLP
1.000 0.080 5 111073369 5 prime UTR variant C/A;G;T snv 3
rs2419621
ACSL5
0.925 0.080 10 112375255 non coding transcript exon variant C/T snv 0.23 3
rs2605100
LOC107985272 ; LYPLAL1-AS1
1.000 0.080 1 219470882 intergenic variant A/G snv 0.77 3
rs28932472
POMC
0.925 0.080 2 25161179 missense variant G/C snv 2.7E-03 2.8E-03 3
rs35568725
PLIN2
0.925 0.080 9 19119676 missense variant A/G snv 4.1E-02 4.0E-02 3
rs3748024
CHCHD5
0.925 0.080 2 112588836 3 prime UTR variant C/G snv 0.41 0.35 3
rs3801266
NAMPT
0.925 0.080 7 106283804 intron variant T/C snv 0.26 3
rs512535
APOB
0.925 0.080 2 21044910 upstream gene variant T/C snv 0.45 3
rs6752378 1.000 0.080 2 24927247 intergenic variant C/A snv 0.57 3
rs7190492
FTO
1.000 0.080 16 53794840 intron variant A/G snv 0.68 3
rs724159998
LEP
0.882 0.080 7 128254557 missense variant G/A;T snv 4.0E-06 3
rs757139012
SIM1
0.882 0.080 6 100390522 missense variant T/C snv 8.0E-06; 4.0E-06 1.4E-05 3
rs774006043
ZPR1 ; APOA5
0.925 0.080 11 116790561 missense variant C/T snv 3
rs8179183
LEPR
1.000 0.080 1 65610269 missense variant G/C;T snv 3
rs9302652
FTO
1.000 0.080 16 53832063 intron variant C/T snv 0.74 3
rs9923544
FTO
1.000 0.080 16 53768073 intron variant C/T snv 0.42 3